FDA Device recall Z-0988-2020
Jamshidi Bone Marrow Aspiration Needle Item Number: 00-1103-007-00
- FDA Device
- Class II
- terminated
- Published 2020-02-12
On 2020-02-12 the FDA classified a Class II recall of Jamshidi Bone Marrow Aspiration Needle Item Number: 00-1103-007-00 by Zimmer Biomet, citing potential for the expiration date on the outer label that was applied by Zimmer Biomet to exceed the expiration date on the inner label.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0988-2020 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2019-12-23 |
| Published | 2020-02-12 |
| Last updated | 2026-09-13 11:55 UTC |
| Company | Zimmer Biomet |
| Distribution | US |
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
Identifiers
| code_info | Lot Numbers : 62754464, 62904231, 63060634 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:55 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0988-2020%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.