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Sign in to claim this brandJoerns Healthcare
US
Last updated September 17, 2026
About
Joerns is a leading partner in long-term post-acute care (LTPAC), providing access to high-quality products with renowned efficacy and safety
From the manufacturer's own website. Source
Information
- Country
- US
- Address
- 2430 Whitehall Park Dr Ste 700, Charlotte, NC, 28273
- Website
- www.joerns.com/
- —
- Phone
- —
- PRRC Contact
- —
- EUDAMED SRN
- —
- FDA FEI Number
- 3012392312
- DUNS Number
- —
Catalogue (540)
Page 1 of 11| Device | Model / Reference | Registries | Class | Status |
|---|---|---|---|---|
| ProMatt Plus | PMP3680NZBA | FDA UDI | Class II | Active |
| WeCare Response Bed | WECC42-T-QO | FDA UDI | Class II | Active |
| Flap Cair LAL Control Unit | FC-CU | FDA UDI | Class II | Active |
| Dolphin Fluid Immersion Simulation | DLPH-3582OO4WJ-M | FDA UDI | Class II | Active |
| Ucxt | XTULHF80GRA | FDA UDI | Class II | Active |
| Apex | SS-HSP | FDA UDI | Class I | Active |
| Panacea 1000 | PAN1000-FLEX-RILQS | FDA UDI | Class II | Active |
| Slings | 50022 | FDA UDI | Class I | Active |
| ProMatt Plus | PMP3680SZBA-C | FDA UDI | Class II | Active |
| Accessories | N352AL | FDA UDI | Class II | Active |
| Accessories | N190 | FDA UDI | Class II | Active |
| Slings | NA1002P | FDA UDI | Class I | Active |
| Ucxt | PANEL-XT-ADVTRDQO | FDA UDI | Class II | Active |
| Joerns DermaFloat LR Mattress | DermaFloat LR | FDA UDI | Class II | Active |
| Slings | NA13498N | FDA UDI | Class I | Active |
| Dolphin | DLPH-OOOOOOUKJ-CU | FDA UDI | Class II | Active |
| Slings | 70056 | FDA UDI | Class I | Active |
| Slings | 113-D-LC | FDA UDI | Class I | Active |
| Dolphin Fluid Immersion Simulation | DLPH-4282LPOOJ-M | FDA UDI | Class II | Active |
| Foam Products | 4815EA | FDA UDI | Class I | Active |
| Slings | WECC-WECARE-H-RIL | FDA UDI | Class I | Active |
| Dolphin Fluid Immersion Simulation | DLPH-3592EXOOJ-M | FDA UDI | Class II | Active |
| WeCare Response Bed | WECC42-T-NM-CO | FDA UDI | Class II | Active |
| Slings | NA1101 | FDA UDI | Class I | Active |
| ProMatt Plus | PMP-CU-04 | FDA UDI | Class I | Active |
| ClimateCare | 48" | FDA UDI | Class II | Active |
| Apex Lifts | HML400-70052 | FDA UDI | Class I | Active |
| Slings | NA25705 | FDA UDI | Class I | Active |
| Apex Lifts | C-HLA-117DLC | FDA UDI | Class I | Active |
| Apex Lifts | HML400-70002 | FDA UDI | Class I | Active |
| Slings | NA26914 | FDA UDI | Class I | Active |
| Dolphin FIS | DLPP-2850CBJ-M | FDA UDI | Class II | Active |
| Ecs | PANEL-ECS6TRDSP | FDA UDI | Class II | Active |
| Slings | NA1050P | FDA UDI | Class I | Active |
| DermaFloat LR Control Unit | Dermafloat LR | FDA UDI | Class II | Active |
| ProCair Plus | 222-4280 | FDA UDI | Class II | Active |
| Slings | NA1068 | FDA UDI | Class I | Active |
| Slings | NA1053P | FDA UDI | Class I | Active |
| Dolphin Fluid Immersion Simulation | DLPH-4282LPOOJ-M | FDA UDI | Class II | Active |
| Dolphin Fluid Immersion Simulation | DLPH-3582LPOOOJ-M | FDA UDI | Class II | Active |
| Slings | NA1606 | FDA UDI | Class I | Active |
| Cair 1000 | Cair LAL | FDA UDI | Class II | Active |
| RC CareChair 850 | RCCC850B | FDA UDI | Class I | Active |
| WeCare Response Bed | WECC-TRD-QO-QSR-CO | FDA UDI | Class II | Active |
| Dolphin Fluid Immersion Simulation | DLPH-3582OOOOJ-M | FDA UDI | Class II | Active |
| Dolphin | DLPH-OOOOOOSWJ-CU | FDA UDI | Class II | Active |
| WeCare Response Bed | WECC-TRD-NM-FSR-BA | FDA UDI | Class II | Active |
| Apex Lifts | 0Y0341 | FDA UDI | Class I | Active |
| Slings | NA25573 | FDA UDI | Class I | Active |
| PrevaMatt | 253-3680 | FDA UDI | Class I | Active |
Related Companies
Authorised Representatives
No authorised representatives on record.
Importers
Not available yet.
Notified Bodies
Not available yet.
Authorities
Not available yet.
FDA Recalls (5)
Recalls reported by this firm to the FDA. Listed at company level — FDA recall records don't identify a specific catalogue device.
| Date | Recall No. | Class | Status | Reason |
|---|---|---|---|---|
| May 3, 2018 | Z-2033-2018 | — | terminated | Joerns Healthcare has identified a potential issue with some of the P.R.O. Matt and ProCair Mattresses. For the identified serial number range of P.R.O. Matt and ProCair Mattresses incorrect connectors (part #s 206-0401 & 206-0405) were provided by a Joerns supplier without the required internal shutoff valves, these shutoff valves prevent air from escaping from the mattress air cells. |
| May 3, 2018 | Z-2034-2018 | — | terminated | Joerns Healthcare has identified a potential issue with some of the P.R.O. Matt and ProCair Mattresses. For the identified serial number range of P.R.O. Matt and ProCair Mattresses incorrect connectors (part #s 206-0401 & 206-0405) were provided by a Joerns supplier without the required internal shutoff valves, these shutoff valves prevent air from escaping from the mattress air cells. |
| Sep 24, 2014 | Z-0151-2015 | — | terminated | The Easy-Care Care-Lock feature installed at the foot of the bed may potentially fail to stay engaged (locked) after the Care-Lock System has been engaged by stepping on the red (locked) pedal. |
| Feb 21, 2007 | Z-0727-2007 | — | terminated | Unapproved Design Change (by base supplier) consisting of a reduction in the number of mast-to-base welds (from four welds to two welds). |
| Jan 6, 2006 | Z-0904-06 | — | terminated | A field correction is being conducted on select models of Hoyer Patient Lifts because of hydraulic jack problems that have resulted in patient injury. The possibility exists that the mounting stud located in the bottom of the hydraulic jack could become loose allowing the jack to disengage from the mast of the lift. |