Z-3252-2018 Class II Terminated
FDA device recall Z-3252-2018 was initiated by Zimmer Biomet, Inc. on Aug 3, 2018 and is designated Class II. Reason for recall: Expiration date incorrectly listed on the label The recall status is terminated (terminated Apr 10, 2020). Affected quantity: 217 units.
Recall Details
- Product Type
- Devices
- Report Date
- Oct 3, 2018
- Initiation Date
- Aug 3, 2018
- Termination Date
- Apr 10, 2020
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 217 units
Product Description
Biomet Sports Medii cine Juggerknot Long Flex Drill Bit with Sleeve Nitinol intended to be used for soft tissue to bone fixation with indications for use in: Shoulder, Foot and Ankle, Knee, Hand and Wrist and Hip repair.Stainless Steel, Sterile Item Number: 110016992
Reason for Recall
Expiration date incorrectly listed on the label
Distribution Pattern
AZ CO FL FL GA LA MA MA MO NY SC TX
Code Information
Lot Numbers: 053940, 545740, 067490, 664610, 165770, 676180, 165830, 688250, 415590, 860050
Source
- Dataset
- openFDA device recall enforcement reports
- FDA record
- This recall in openFDA (JSON)
- Enforcement Report
- Search FDA's Enforcement Report for Z-3252-2018
- openFDA file date
- Oct 23, 2026
- Loaded by RegDataLab
- Oct 24, 2026