Z-0988-2020 Class II Terminated
FDA device recall Z-0988-2020 was initiated by Zimmer Biomet, Inc. on December 23, 2019 and is designated Class II. 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 The recall status is terminated (terminated September 10, 2020). Affected quantity: 133 units.
Recall Details
- Product Type
- Devices
- Report Date
- February 12, 2020
- Initiation Date
- December 23, 2019
- Termination Date
- September 10, 2020
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 133 units
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
Distribution Pattern
US Nationwide
Code Information
Lot Numbers : 62754464, 62904231, 63060634