Z-2245-2018 Class II Terminated
FDA device recall Z-2245-2018 was initiated by Synthes (USA) Products LLC on Mar 5, 2018 and is designated Class II. Reason for recall: Affected screw gauges incorrectly measure screws 5.41mm shorter than the actual overall screw length. The recall status is terminated (terminated Feb 28, 2020). Affected quantity: 7.
Recall Details
- Product Type
- Devices
- Report Date
- Jun 27, 2018
- Initiation Date
- Mar 5, 2018
- Termination Date
- Feb 28, 2020
- Voluntary/Mandated
- Voluntary: Firm initiated
- Product Quantity
- 7
Product Description
Part no. 690.375, Graphic Case F/6.5mm & 7.3mm Combined Cannulated Screw Set
Reason for Recall
Affected screw gauges incorrectly measure screws 5.41mm shorter than the actual overall screw length.
Distribution Pattern
Distributed to accounts in CA, IL, IN, KS, LA, MD, NC, NE, NJ, OR, TX, and VA. Foreign distribution to Canada.
Code Information
FL00860
Source
- Dataset
- openFDA device recall enforcement reports
- FDA record
- This recall in openFDA (JSON)
- Enforcement Report
- Search FDA's Enforcement Report for Z-2245-2018
- openFDA file date
- Oct 26, 2026
- Loaded by RegDataLab
- Oct 27, 2026