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J. T. Posey Co.

Country not established

Devices
13
FDA recalls
25

At a glance

Counted by deviCERTS from registry records

Market reach

United States
FDA recalls

What J. T. Posey Co. makes

The company manufactures physical restraint devices for medical and institutional use, including bed restraints, limb holders, straight jackets, jackets and vests, pelvic holders, multiple belts, and accessories like sitter systems and laptop trays. These products are designed to secure patients or individuals in seated or supine positions, often in clinical or long-term care settings.

All listed devices fall under Class I regulatory classification in the US, with some models supported by FDA 510(k) clearance. The portfolio is registered under the FDA’s 510(k) pathway, and the manufacturer operates from the United States.

AI-generated from registry data, 2 Oct 2026. Not verified by deviCERTS or the manufacturer.

Catalogue13

Newest first, rows 1-13 of 13

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  • Posey Bed Ref K113355

    Class I
    Active 510(k) 510(k) I

  • Pediatric Limb Holders Ref K963439

    Class I
    Active 510(k) 510(k) I

  • Posey Straight Jackets Ref K963410

    Class I
    Active 510(k) 510(k) I

  • Jackets And Vests Ref K963442

    Class I
    Active 510(k) 510(k) I

  • Restraint Accessories Ref K963436

    Class I
    Active 510(k) 510(k) I

  • Posey Bed Ref K113357

    Class I
    Active 510(k) 510(k) I

  • Pelvic Holders Ref K963437

    Class I
    Active 510(k) 510(k) I

  • Multiple Belts Ref K963414

    Class I
    Active 510(k) 510(k) I

  • Posey Sitter Ref K920206

    Class I
    Active 510(k) 510(k) I

  • Posey Bed Ref K103817

    Class I
    Active 510(k) 510(k) I

  • Posey Laptop Trays Ref K963411

    Class I
    Active 510(k) 510(k) I

  • Multiple Limb Holders Ref K963413

    Class I
    Active 510(k) 510(k) I

  • Posey Hugger Ref K963409

    Class I
    Active 510(k) 510(k) I

Rows 1-13 of 13

FDA recalls25

Recalls are matched to the firm by name. FDA recall data as of 22 Oct 2026.

Showing the 10 most recent of 25 recalls.

  • 2012

    • 31 Oct 2012 Z-1071-2013 Class II Terminated The firm voluntarily recalled Biothane Restraint Cuffs, Catalog No. 2900, that did not meet the required specifications for tensile strength. Failure of these rivets could allow the cuff to become disconnected from the connecting strap and allow patients to regain free use of the limb. Distribution: Nationwide Distribution

  • 2009

    • 20 Apr 2009 Z-2254-2009 Unclassified (pre-2012) Terminated Posey has initiated a recall on certain Posey product units which were manufactured using an incorrect key lock buckle. The intended use of these products is to limit a patient's movement to the extent necessary for treatment, examination or protection of the patient or others. Distribution: Class II Recall - Worldwide Distribution -- United States, Canada, France, Belgium and the Netherlands. Submission number: K963436
    • 20 Apr 2009 Z-2255-2009 Unclassified (pre-2012) Terminated Posey has initiated a recall on certain Posey product units which were manufactured using an incorrect key lock buckle. The intended use of these products is to limit a patient's movement to the extent necessary for treatment, examination or protection of the patient or others. Distribution: Class II Recall - Worldwide Distribution -- United States, Canada, France, Belgium and the Netherlands. Submission number: K963436
    • 20 Apr 2009 Z-2256-2009 Unclassified (pre-2012) Terminated Posey has initiated a recall on certain Posey product units which were manufactured using an incorrect key lock buckle. The intended use of these products is to limit a patient's movement to the extent necessary for treatment, examination or protection of the patient or others. Distribution: Class II Recall - Worldwide Distribution -- United States, Canada, France, Belgium and the Netherlands. Submission number: K963436
    • 20 Apr 2009 Z-2257-2009 Unclassified (pre-2012) Terminated Posey has initiated a recall on certain Posey product units which were manufactured using an incorrect key lock buckle. The intended use of these products is to limit a patient's movement to the extent necessary for treatment, examination or protection of the patient or others. Distribution: Class II Recall - Worldwide Distribution -- United States, Canada, France, Belgium and the Netherlands. Submission number: K963436
    • 20 Apr 2009 Z-2258-2009 Unclassified (pre-2012) Terminated Posey has initiated a recall on certain Posey product units which were manufactured using an incorrect key lock buckle. The intended use of these products is to limit a patient's movement to the extent necessary for treatment, examination or protection of the patient or others. Distribution: Class II Recall - Worldwide Distribution -- United States, Canada, France, Belgium and the Netherlands. Submission number: K963436
    • 20 Apr 2009 Z-2259-2009 Unclassified (pre-2012) Terminated Posey has initiated a recall on certain Posey product units which were manufactured using an incorrect key lock buckle. The intended use of these products is to limit a patient's movement to the extent necessary for treatment, examination or protection of the patient or others. Distribution: Class II Recall - Worldwide Distribution -- United States, Canada, France, Belgium and the Netherlands. Submission number: K963436
    • 20 Apr 2009 Z-2260-2009 Unclassified (pre-2012) Terminated Posey has initiated a recall on certain Posey product units which were manufactured using an incorrect key lock buckle. The intended use of these products is to limit a patient's movement to the extent necessary for treatment, examination or protection of the patient or others. Distribution: Class II Recall - Worldwide Distribution -- United States, Canada, France, Belgium and the Netherlands. Submission number: K963436
    • 20 Apr 2009 Z-2261-2009 Unclassified (pre-2012) Terminated Posey has initiated a recall on certain Posey product units which were manufactured using an incorrect key lock buckle. The intended use of these products is to limit a patient's movement to the extent necessary for treatment, examination or protection of the patient or others. Distribution: Class II Recall - Worldwide Distribution -- United States, Canada, France, Belgium and the Netherlands. Submission number: K963436
    • 20 Apr 2009 Z-2262-2009 Unclassified (pre-2012) Terminated Posey has initiated a recall on certain Posey product units which were manufactured using an incorrect key lock buckle. The intended use of these products is to limit a patient's movement to the extent necessary for treatment, examination or protection of the patient or others. Distribution: Class II Recall - Worldwide Distribution -- United States, Canada, France, Belgium and the Netherlands. Submission number: K963436
Show all 25 recalls

  • 2009

    • 20 Apr 2009 Z-2263-2009 Unclassified (pre-2012) Terminated Posey has initiated a recall on certain Posey product units which were manufactured using an incorrect key lock buckle. The intended use of these products is to limit a patient's movement to the extent necessary for treatment, examination or protection of the patient or others. Distribution: Class II Recall - Worldwide Distribution -- United States, Canada, France, Belgium and the Netherlands. Submission number: K963436
    • 20 Apr 2009 Z-2264-2009 Unclassified (pre-2012) Terminated Posey has initiated a recall on certain Posey product units which were manufactured using an incorrect key lock buckle. The intended use of these products is to limit a patient's movement to the extent necessary for treatment, examination or protection of the patient or others. Distribution: Class II Recall - Worldwide Distribution -- United States, Canada, France, Belgium and the Netherlands. Submission number: K963436
    • 20 Apr 2009 Z-2265-2009 Unclassified (pre-2012) Terminated Posey has initiated a recall on certain Posey product units which were manufactured using an incorrect key lock buckle. The intended use of these products is to limit a patient's movement to the extent necessary for treatment, examination or protection of the patient or others. Distribution: Class II Recall - Worldwide Distribution -- United States, Canada, France, Belgium and the Netherlands. Submission number: K963436
    • 20 Apr 2009 Z-2266-2009 Unclassified (pre-2012) Terminated Posey has initiated a recall on certain Posey product units which were manufactured using an incorrect key lock buckle. The intended use of these products is to limit a patient's movement to the extent necessary for treatment, examination or protection of the patient or others. Distribution: Class II Recall - Worldwide Distribution -- United States, Canada, France, Belgium and the Netherlands. Submission number: K963436
    • 20 Apr 2009 Z-2267-2009 Unclassified (pre-2012) Terminated Posey has initiated a recall on certain Posey product units which were manufactured using an incorrect key lock buckle. The intended use of these products is to limit a patient's movement to the extent necessary for treatment, examination or protection of the patient or others. Distribution: Class II Recall - Worldwide Distribution -- United States, Canada, France, Belgium and the Netherlands. Submission number: K963436
    • 20 Apr 2009 Z-2268-2009 Unclassified (pre-2012) Terminated Posey has initiated a recall on certain Posey product units which were manufactured using an incorrect key lock buckle. The intended use of these products is to limit a patient's movement to the extent necessary for treatment, examination or protection of the patient or others. Distribution: Class II Recall - Worldwide Distribution -- United States, Canada, France, Belgium and the Netherlands. Submission number: K963436
    • 20 Apr 2009 Z-2269-2009 Unclassified (pre-2012) Terminated Posey has initiated a recall on certain Posey product units which were manufactured using an incorrect key lock buckle. The intended use of these products is to limit a patient's movement to the extent necessary for treatment, examination or protection of the patient or others. Distribution: Class II Recall - Worldwide Distribution -- United States, Canada, France, Belgium and the Netherlands. Submission number: K963436
    • 20 Apr 2009 Z-2270-2009 Unclassified (pre-2012) Terminated Posey has initiated a recall on certain Posey product units which were manufactured using an incorrect key lock buckle. The intended use of these products is to limit a patient's movement to the extent necessary for treatment, examination or protection of the patient or others. Distribution: Class II Recall - Worldwide Distribution -- United States, Canada, France, Belgium and the Netherlands. Submission number: K963436
    • 20 Apr 2009 Z-2271-2009 Unclassified (pre-2012) Terminated Posey has initiated a recall on certain Posey product units which were manufactured using an incorrect key lock buckle. The intended use of these products is to limit a patient's movement to the extent necessary for treatment, examination or protection of the patient or others. Distribution: Class II Recall - Worldwide Distribution -- United States, Canada, France, Belgium and the Netherlands. Submission number: K963436
    • 20 Apr 2009 Z-2272-2009 Unclassified (pre-2012) Terminated Posey has initiated a recall on certain Posey product units which were manufactured using an incorrect key lock buckle. The intended use of these products is to limit a patient's movement to the extent necessary for treatment, examination or protection of the patient or others. Distribution: Class II Recall - Worldwide Distribution -- United States, Canada, France, Belgium and the Netherlands. Submission number: K963436
    • 20 Apr 2009 Z-2273-2009 Unclassified (pre-2012) Terminated Posey has initiated a recall on certain Posey product units which were manufactured using an incorrect key lock buckle. The intended use of these products is to limit a patient's movement to the extent necessary for treatment, examination or protection of the patient or others. Distribution: Class II Recall - Worldwide Distribution -- United States, Canada, France, Belgium and the Netherlands. Submission number: K963436
    • 20 Apr 2009 Z-2274-2009 Unclassified (pre-2012) Terminated Posey has initiated a recall on certain Posey product units which were manufactured using an incorrect key lock buckle. The intended use of these products is to limit a patient's movement to the extent necessary for treatment, examination or protection of the patient or others. Distribution: Class II Recall - Worldwide Distribution -- United States, Canada, France, Belgium and the Netherlands. Submission number: K963436
    • 20 Apr 2009 Z-2275-2009 Unclassified (pre-2012) Terminated Posey has initiated a recall on certain Posey product units which were manufactured using an incorrect key lock buckle. The intended use of these products is to limit a patient's movement to the extent necessary for treatment, examination or protection of the patient or others. Distribution: Class II Recall - Worldwide Distribution -- United States, Canada, France, Belgium and the Netherlands. Submission number: K963436

  • 2008

    • 8 Sep 2008 Z-0934-2009 Unclassified (pre-2012) Terminated The recall was initiated after an investigation conducted by the Posey Company determined that a patient may be able to catch the belt on a stationary object (wall, pipe, etc.) and use their body force to tear or break the strap, creating freedom of arm movement. In some patient populations, such freedom of movement could pose an unwanted hazard of serious injury to a patient or caregiver. Distribution: Worldwide Distribution including USA and countries of Australia, Belgium, Canada, France, Germany, Ireland, Italy,…
      Full distribution text Worldwide Distribution including USA and countries of Australia, Belgium, Canada, France, Germany, Ireland, Italy, Korea, Lithuania and Netherlands.
      Submission number: K963413
    • 25 Jul 2008 Z-0286-2009 Unclassified (pre-2012) Terminated Failure to restrain: This recall was initiated after a complaint was received by the firm regarding a Posey 2217SL unit indicating that a patient was able to pull the rivet or washer through the synthetic leather allowing the patient to have freedom of arm movement. A second complaint was received indicating that a patient was able to tear the strap at the adjustment notch on a Posey 221 7SL unit Distribution: Worldwide, USA, Australia, Canada, France & The Netherlands. Submission number: K963413

Frequently asked questions

How many devices does J. T. Posey Co. have in the registry?

The registry currently lists 13 devices for J. T. Posey Co.. Devices recorded under merged duplicate company entries are counted once.

Which registries list J. T. Posey Co.'s devices?

Among its 13 most recently registered devices, J. T. Posey Co. has devices listed in FDA 510(k) (13 devices).

What risk classes do J. T. Posey Co.'s devices fall under?

Among its 13 most recently registered devices, the classes recorded for J. T. Posey Co.'s devices are Class I. Each device page shows its own class and authorisation.

Are there FDA recall records for J. T. Posey Co.?

FDA recall records list 25 recalls initiated by J. T. Posey Co., the most recent initiated on 2012-10-31. A recall is often a precaution started by the manufacturer; the records say nothing about the company's overall record.

What are the newest devices from J. T. Posey Co. in the registry?

The most recently registered devices listed for J. T. Posey Co. include POSEY BED, PEDIATRIC LIMB HOLDERS, POSEY STRAIGHT JACKETS and JACKETS AND VESTS.

Generated automatically from registry data and not verified by a human reviewer.