1.5 mm Rapid Resorb Orbt1 F1 P1 w/Bending Template / 24 mm - Sterile, Rapid Resorbable Fixation System. 1.5 mm Rapid Res
FDA device recall Z-1918-2016 · posted 2016-06-07 · Terminated
Recall details
- Recalling firm
- Synthes (USA) Products LLC
- Reason for recall
- Labeling errors. The outer packge label expiration date may exceed the expiration date of the subcomponents.
- Action taken
- DePuy Synthes sent an Urgent Medical Device Recall Notice dated May 2, 2016, to all affected customers. The notice identified the product, the problem, and the action to be taken by the customer. Customers were instructed to review their inventory immediately and remove the affected lots from their stock. Customers were instructed to call 1-800-479-6329 to obtain a Return Authorization (RA) Number and replacement product., customers were also asked to complete the Verification Section and scan/email to Synthes4096@stericycle.com. Customers with questions were instructed to call 610-719-5450.
- Root cause
- Under Investigation by firm
- Status
- Terminated
- Product code
- JEY
- Quantity affected
- 22 units
- Distribution
- Nationwide Distribution to DE, NC, CA, OK, PA, SC, WI, CO, NJ, TX, UT, IL, MO, MI, AL, KS.
- Date initiated
- 2016-05-02
- Date posted
- 2016-06-07
- Date terminated
- 2016-12-09
- Location
- West Chester, PA
Monitor recalls programmatically
Recalls and clearances share one API, with change alerts when new recalls post.
Related 510(k) clearances
| Record | Firm | Date |
|---|---|---|
| SYNTHES (USA) RAPID RESORBABLE FIXATION SYSTEM (K062789) | Synthes (Usa) | 2007-02-27 |
| SYNTHES POLY (L-LACTIDE-CO-GLYCOLIDE) RESORBABLE FIXATION SYSTEM (K030069) | Synthes (Usa) | 2003-04-08 |