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.