International Medsurg Connection
Country not established
- Devices
- 13
- FDA recalls
- 65
At a glance
Market reach
- United States
- FDA recalls
What International Medsurg Connection makes
International Medsurg Connection manufactures single-use surgical and medical devices, including irrigation sets, hypodermic and insulin syringes, blood collection needles, surgical drapes, hypodermic needles, surgical face masks, and equipment covers for medical procedures.
The company’s portfolio consists of Class II medical devices, all of which are listed under the FDA’s 510(k) pathway. These devices are regulated under U.S. federal law and are intended for use in surgical and procedural settings.
Catalogue
Search and filter all 13 devicesFDA recalls
FDA recall records list 65 recalls initiated by International Medsurg Connection, the earliest on 2006-08-16 and the most recent on 2017-06-23. By recorded status: 65 terminated. The reasons filed fall into these groups: labeling or instructions for use and sterility or contamination. A recall is often a precaution started by the manufacturer, and a count of records is not a verdict on a company.
Recalls initiated per year
- 2017 59
- 2018 0
- 2019 0
- 2020 0
- 2021 0
- 2022 0
- 2023 0
- 2024 0
- 2025 0
- 2026 0
2017
- 23 Jun 2017 Z-2804-2017 Class II Terminated Insufficient documentation to support product sterility claims.
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- 23 Jun 2017 Z-2805-2017 Class II Terminated Insufficient documentation to support product sterility claims.
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- 23 Jun 2017 Z-2806-2017 Class II Terminated Insufficient documentation to support product sterility claims.
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- 23 Jun 2017 Z-2807-2017 Class II Terminated Insufficient documentation to support product sterility claims.
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- 23 Jun 2017 Z-2808-2017 Class II Terminated Insufficient documentation to support product sterility claims.
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- 23 Jun 2017 Z-2809-2017 Class II Terminated Insufficient documentation to support product sterility claims.
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- 23 Jun 2017 Z-2810-2017 Class II Terminated Insufficient documentation to support product sterility claims.
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- 23 Jun 2017 Z-2811-2017 Class II Terminated Insufficient documentation to support product sterility claims.
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- 23 Jun 2017 Z-2812-2017 Class II Terminated Insufficient documentation to support product sterility claims.
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- 23 Jun 2017 Z-2813-2017 Class II Terminated Insufficient documentation to support product sterility claims.
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- 23 Jun 2017 Z-2804-2017 Class II Terminated Insufficient documentation to support product sterility claims.
Show the 25 most recent of 65 recalls
2017
- 23 Jun 2017 Z-2814-2017 Class II Terminated Insufficient documentation to support product sterility claims.
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- 23 Jun 2017 Z-2815-2017 Class II Terminated Insufficient documentation to support product sterility claims.
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- 23 Jun 2017 Z-2816-2017 Class II Terminated Insufficient documentation to support product sterility claims.
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- 23 Jun 2017 Z-2817-2017 Class II Terminated Insufficient documentation to support product sterility claims.
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- 23 Jun 2017 Z-2818-2017 Class II Terminated Insufficient documentation to support product sterility claims.
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- 23 Jun 2017 Z-2819-2017 Class II Terminated Insufficient documentation to support product sterility claims.
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- 23 Jun 2017 Z-2820-2017 Class II Terminated Insufficient documentation to support product sterility claims.
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- 23 Jun 2017 Z-2821-2017 Class II Terminated Insufficient documentation to support product sterility claims.
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- 23 Jun 2017 Z-2822-2017 Class II Terminated Insufficient documentation to support product sterility claims.
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- 23 Jun 2017 Z-2823-2017 Class II Terminated Insufficient documentation to support product sterility claims.
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- 23 Jun 2017 Z-2824-2017 Class II Terminated Insufficient documentation to support product sterility claims.
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- 23 Jun 2017 Z-2825-2017 Class II Terminated Insufficient documentation to support product sterility claims.
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- 23 Jun 2017 Z-2826-2017 Class II Terminated Insufficient documentation to support product sterility claims.
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- 23 Jun 2017 Z-2827-2017 Class II Terminated Insufficient documentation to support product sterility claims.
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- 23 Jun 2017 Z-2828-2017 Class II Terminated Insufficient documentation to support product sterility claims.
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- 23 Jun 2017 Z-2814-2017 Class II Terminated Insufficient documentation to support product sterility claims.
Frequently asked questions
How many devices does International Medsurg Connection have in the registry?
The registry currently lists 13 devices for International Medsurg Connection. Devices recorded under merged duplicate company entries are counted once.
Which registries list International Medsurg Connection's devices?
Among its 13 most recently registered devices, International Medsurg Connection has devices listed in FDA 510(k) (13 devices).
What risk classes do International Medsurg Connection's devices fall under?
Among its 13 most recently registered devices, the classes recorded for International Medsurg Connection's devices are Class II. Each device page shows its own class and authorisation.
Are there FDA recall records for International Medsurg Connection?
FDA recall records list 65 recalls initiated by International Medsurg Connection, the most recent initiated on 2017-06-23. 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 International Medsurg Connection in the registry?
The most recently registered devices listed for International Medsurg Connection include IRRIGATION SETS, IMC SURGICAL DRAPE, IMC HYPODERMIC NEEDLE and MEDSURG EQUIPMENT COVERS.