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Recall data is sourced from official U.S. government agencies (CPSC, FDA, NHTSA, USDA) and processed using AI to improve readability. This site is not affiliated with or endorsed by any government agency. Always refer to the original agency notice for authoritative information.

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Medium RiskFDA Device
Medical Devices/Implants & Prosthetics

TriMed Inc.: Volar Bearing Plates Recalled Due to Bearings Popping Out During Surgery

Agency Publication Date: January 31, 2024
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Summary

TriMed Inc. has recalled 270 Volar Bearing Plates, which are used in surgical wrist fixation systems to treat fractures and bone issues. These medical devices are being recalled because the bearings used to secure the plates during surgery may pop out from the peg holes. If you have a wrist surgery scheduled or have recently undergone one involving these plates, you should contact your healthcare provider to discuss your treatment.

Risk

The bearings can dislodge from the peg holes during surgical installation, which could compromise the stability of the wrist fixation or require additional surgical intervention to correct the issue.

What You Should Do

  1. Contact your healthcare provider immediately if you have recently undergone wrist surgery to determine if a TriMed Volar Bearing Plate was used in your procedure.
  2. Hospital staff and surgeons should check their inventory for Volar Bearing Plates with the following REF numbers: VBEAL-3-7N, VBEAL-5-7N, VBEAL-3-7S, VBEAL-5-7S, VBEAL-7-7S, VBEAL-3-7W, VBEAL-5-7W, VBEAR-3-7N, VBEAR-5-7-N, VBEAR-3-7S, VBEAR-5-7S, VBEAR-7-7S, VBEAR-3-7W, and VBEAR-5-7W.
  3. Verify affected lots against your stock, specifically looking for lot numbers such as ME23071, ME23072, ME23073, ME23031, ME23067, ME23082, ME23097, ME23068, ME23004, ME23086, ME23033, ME23036, ME23069, ME23084, ME23085, ME23074, ME23029, ME23087, ME23019, ME23022, ME23034, ME23041, and ME23037.
  4. Contact TriMed Inc. at their Santa Clarita, California office for specific instructions regarding the return or replacement of these surgical plates.
  5. For additional information or to report any issues, contact the FDA directly at 1-888-463-6332 (1-888-INFO-FDA) or visit www.fda.gov/medical-devices/medical-device-recalls.

Your Remedy Options

๐Ÿ“‹Other Action

manufacturer or healthcare provider Contact

How to: Contact your healthcare provider or the manufacturer for further instructions and potential refund

Affected Products

Product: Volar Bearing Plate (VBEAL-3-7N)
Model / REF:
VBEAL-3-7N
UPC Codes:
00842188124907
Lot Numbers:
ME23071
ME23072
Product: Volar Bearing Plate (VBEAL-5-7N)
Model / REF:
VBEAL-5-7N
UPC Codes:
00842188124914
Lot Numbers:
ME23073
Product: Volar Bearing Plate (VBEAL-3-7S)
Model / REF:
VBEAL-3-7S
UPC Codes:
00842188124938
Lot Numbers:
ME23031
ME23067
ME23082
ME23097
Product: Volar Bearing Plate (VBEAL-5-7S)
Model / REF:
VBEAL-5-7S
UPC Codes:
00842188124945
Lot Numbers:
ME23068
Product: Volar Bearing Plate (VBEAL-7-7S)
Model / REF:
VBEAL-7-7S
UPC Codes:
00842188124952
Lot Numbers:
ME23004
ME23086
Product: Volar Bearing Plate (VBEAL-3-7W)
Model / REF:
VBEAL-3-7W
UPC Codes:
00842188124969
Lot Numbers:
ME23033
Product: Volar Bearing Plate (VBEAL-5-7W)
Model / REF:
VBEAL-5-7W
UPC Codes:
00842188124976
Lot Numbers:
ME23036
Product: Volar Bearing Plate (VBEAR-3-7N)
Model / REF:
VBEAR-3-7N
UPC Codes:
00842188124990
Lot Numbers:
ME23069
ME23084
ME23085
Product: Volar Bearing Plate (VBEAR-5-7-N)
Model / REF:
VBEAR-5-7-N
UPC Codes:
00842188125003
Lot Numbers:
ME23074
Product: Volar Bearing Plate (VBEAR-3-7S)
Model / REF:
VBEAR-3-7S
UPC Codes:
00842188125027
Lot Numbers:
ME23029
ME23087
Product: Volar Bearing Plate (VBEAR-5-7S)
Model / REF:
VBEAR-5-7S
UPC Codes:
00842188125034
Lot Numbers:
ME23019
Product: Volar Bearing Plate (VBEAR-7-7S)
Model / REF:
VBEAR-7-7S
UPC Codes:
00842188125041
Lot Numbers:
ME23022
Product: Volar Bearing Plate (VBEAR-3-7W)
Model / REF:
VBEAR-3-7W
UPC Codes:
00842188125058
Lot Numbers:
ME23034
Product: Volar Bearing Plate (VBEAR-5-7W)
Model / REF:
VBEAR-5-7W
UPC Codes:
00842188125065
Lot Numbers:
ME23041
ME23037

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 93748
Status: Active
Manufacturer: TriMed Inc.
Sold By: hospitals; surgical centers; medical distributors
Manufactured In: United States
Units Affected: 270
Distributed To: Florida, Michigan, Alabama, New York, California

Were You Affected by This Recall?

If you or a family member were harmed by this recalled product, you may have legal rights. Consider consulting a consumer protection attorney to understand your options for compensation.

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This is general information, not legal advice. Go Backs is not a law firm and does not provide legal services.

AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.

Sources: FDA iRES ยท Raw API Response

openFDA Disclaimer: This recall information is sourced from the openFDA API. Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Refer to the openFDA terms of service for more information.