REVERSE PROSTHESIS SHOULDER SYSTEM, SCREW, LOCKING BONE, RSP, 5mmX30mm long, REF: 506-03-130
FDA device recall Z-0098-2024 · posted 2023-10-12 · Open, Classified
Recall details
- Recalling firm
- Encore Medical, LP
- Reason for recall
- Reverse shoulder prosthesis package that should contain 5mmx30 screws could contain incorrect 3.5mmx30 screws. Use of incorrect screws could result in surgical delay and inadequate fixation.
- Action taken
- On 8/22/23, recall notices were emailed to agents and registration holders who were asked to do the following: Contact Customer Service at 1-800-456-8696 to assist with return and replacement. This notice needs to be passed on to all those within your organization or to any organization where the potentially affected product has been transferred. Complete and return the acknowledgement and response form. If you have questions, please email productsafety@enovis.com
- Root cause
- Mixed-up of materials/components
- Status
- Open, Classified
- Product code
- PHX
- Quantity affected
- 70
- Distribution
- US: FL, IN, WI, IA, MN, KY, NY, AZ, RI, WA, OH, SC, VA, TX. OUS: MX
- Date initiated
- 2023-08-22
- Date posted
- 2023-10-12
- Location
- Austin, TX
Monitor recalls programmatically
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Related 510(k) clearances
| Record | Firm | Date |
|---|---|---|
| ENCORE REVERSE SHOULDER PROSTHESIS (K041066) | Encore Medical L.P. | 2005-03-24 |