2.0 Mandible Locking Plate (MLP) Bender / Cutter (part number 329.143) Intended to be used for...
FDA Device Recall #Z-1021-2015 — Class II — December 15, 2014
Recall Summary
| Recall Number | Z-1021-2015 |
| Classification | Class II — Moderate risk |
| Date Initiated | December 15, 2014 |
| Status | Terminated |
| Voluntary | Voluntary: Firm initiated |
Recalling Firm
| Firm | Synthes, Inc. |
| Location | West Chester, PA |
| Product Type | Devices |
| Quantity | 973 |
Product Description
2.0 Mandible Locking Plate (MLP) Bender / Cutter (part number 329.143) Intended to be used for bending and/or cutting Mandible Locking Plates.
Reason for Recall
Certain lots have the potential for tip breakage while bending 2.0 mm thick plates. If device is used and breaks while in the Operating Room, surgical delay may occur while alternate bending or cutting instruments are located.
Distribution Pattern
Worldwide Distribution -- US and Canada.
Lot / Code Information
Sold Lot Numbers: 4520830 4519339 4528112 4527510 4527509 4528678 4529517 4532428 4542201 4547106 4547107 4548231 4552202 4552203 4562899 4566835 4572774 4572775 4578754 4581035 4593516 4738938 4768238 4805320 4805321 4805622 4805623 4814351 4869678 4871808 4880493 4880495 4888588 4915212 4915213 4935249 4935250 4964319 4964324 4973229 5021231 5021232 5021233 5036650 5036651 5056855 5056154 5056856 5079563 5079564 5079565 5079538 5090675 5090677 5105352 5144695 5144697 5144696 5161969 5161970 5191074 5196260 5229584 5229586 5229585 5229587 5253009 5256476 5256477 5262049 5267000 5276395 5278583 5283776 5283780 5353853 5360628 5367534 5367535 5370545 5388335 5370546 5388336 5765950 5775823; Manufacturing Lot Number A7LA49 A7LA48 A7LA51 A7LA50 A7LA50 A7LA51 A7LA51 A7LA47 A7MA03 A7MA05 A7MA05 A7MA05 A7MA06 A7MA06 A7MA09 A7MA10 A7MA11 A7MA11 A7MA13 A7MA14 A7MA18 A7NA08 A7NA08 A7NA25 A7NA25 A7NA25 A7NA25 A7NA25 A7NA40 A7NA41 A7NA43 A7NA43 A7NA43 A7NA43 A7NA51 A7NA52 A7NA51 A7OA09 A7OA09 A7OA09 A7OA21 A7OA21 A7OA21 A7OA24 A7OA24 A7OA30 A7OA29 A7OA33 A7OA29 A7OA35 A7OA35 A7OA36 A7OA38 A7OA38 A7OA41 A7OA50 A7OA50 A7OA50 A7OA51 A7OA51 A7PA07 A7PA08 A7OA50 A7OA51 A7PA08 A7PA07 A7PA20 A7PA21 A7PA21 A7PA21 A7PA23 A7PA23 A7PA24 A7PA25 A7PA25 A7PA39 A7PA40 A7PA41 A7PA41 A7PA42 A7PA41 A7PA42 A7PA43 A7PA47 A7PA47
Other Recalls from Synthes, Inc.
| Recall # | Classification | Product | Date |
|---|---|---|---|
| Z-2698-2020 | Class II | MatrixNEURO Screws - Product Usage: The intende... | Jun 18, 2020 |
| Z-0880-2020 | Class II | 2.4MM TI VA LOCKING SCREW STARDRIVE 12MM STERIL... | Dec 16, 2019 |
| Z-0883-2020 | Class II | 2.4MM TI VA LOCKING SCREW STARDRIVE 24MM STERIL... | Dec 16, 2019 |
| Z-0879-2020 | Class II | 2.4MM TI VA LOCKING SCREW STARDRIVE 10MM STERIL... | Dec 16, 2019 |
| Z-0881-2020 | Class II | 2.4MM TI VA LOCKING SCREW STARDRIVE 16MM STERIL... | Dec 16, 2019 |
Frequently Asked Questions
Contact your healthcare provider and the device manufacturer immediately. Check whether your specific model number and lot number are included in the recall scope. For external devices, stop using the affected product and arrange a replacement. For implanted devices, do not panic — removal is typically not required unless the risk assessment clearly indicates it. Your physician will guide you based on your individual clinical situation and the FDA's recommended actions. Report any adverse effects you may have experienced to FDA MedWatch at 1-800-FDA-1088.
Class I recalls indicate a reasonable probability of serious adverse health consequences or death from the defect. Class II recalls involve products that may cause temporary or medically reversible adverse health consequences, or where serious consequences are remote. Class III recalls cover products not likely to cause any adverse health consequences, typically involving technical regulatory violations. The classification guides urgency — Class I recalls require immediate action, while Class III may simply involve returning a product or acknowledging a labeling change. Always read the specific recall notice for recommended patient actions.
Report problems with medical devices to the FDA through MedWatch at 1-800-FDA-1088 or online at FDA.gov/safety/medwatch. Healthcare facilities are required by law to report device-related serious injuries and deaths. Patients and consumers can also report voluntarily. Include the device name, manufacturer, model number, and a description of the problem and any patient outcome. Reports from patients and clinicians help the FDA identify emerging safety signals and may trigger investigations that lead to recalls of dangerous devices.
What Should You Do?
Stop using this device if you are affected by this recall. Contact your healthcare provider and the manufacturer immediately for guidance. Report adverse events to FDA MedWatch.