Recall Z-0988-2020— Zimmer Biomet, Inc.
Class II · Terminated
Class II FDA medical device recall by Zimmer Biomet, Inc., initiated 2019-12-23, terminated 2020-09-10. FDA's recall record names no specific 510(k) clearance for this event. Product: Jamshidi Bone Marrow Aspiration Needle Item Number: 00-1103-007-00. Reason: Potential for the expiration date on the outer label that was applied by Zimmer Biomet to exceed the expiration date on the inner label.
- Recalling firm
- Zimmer Biomet, Inc.
- Classification
- Class II
- Status
- Terminated
- Initiated
- 2019-12-23
- Terminated
- 2020-09-10
- Firm location
- Warsaw, IN, United States
Product description
Jamshidi Bone Marrow Aspiration Needle Item Number: 00-1103-007-00
Reason for recall
Potential for the expiration date on the outer label that was applied by Zimmer Biomet to exceed the expiration date on the inner label
Data sourced from openFDA. This site is unofficial and independent of the FDA.