Go Backs
HomeCategoriesStatesCheck Your Home
Go Backs

Track product recalls and safety alerts from CPSC, FDA, NHTSA, and USDA. Stay informed and keep your family safe.

Browse

  • Categories
  • States
  • Check Your Home
  • Risk Levels

Agencies

  • CPSC
  • FDA Food
  • FDA Drug
  • FDA Device
  • FDA Veterinary
  • NHTSA
  • USDA

Company

  • About
  • FAQ
  • Contact
  • Terms of Service
  • Privacy Policy
Buy Me a Coffee

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.

ยฉ 2026 Go Backs. All rights reserved.

Medium RiskFDA Device
Medical Devices/Surgical Equipment

Synthes Bone Taps Recalled for Incorrect Threading

Agency Publication Date: March 30, 2026
Share:
Sign in to monitor this recall

Summary

Synthes (USA) Products LLC is recalling 110 bone tap medical devices because two different product lots were swapped during packaging. The 2.4 VOLT Locking Screw Tap (77 units) and the 2.4 VOLT Cortex Screw Tap (33 units) were placed in the wrong packaging, meaning the tools have the incorrect thread type for their labeled purpose. This issue was discovered by the manufacturer and initiated through a notification letter to affected facilities. Healthcare providers should immediately stop using these specific lots and contact the manufacturer to arrange for a return or swap.

Risk

Using a bone tap with the incorrect thread can lead to improper hole preparation during surgery, potentially causing bone screws to fit poorly, lose stability, or fail to secure properly in the patient's bone.

What You Should Do

  1. Identify if you have the affected bone taps by checking the Part Number, GTIN, and Lot Number on the device packaging.
  2. For the Locking Screw Tap, look for Part Number 03.424.124-US, GTIN 10886982335944, and Lot Number 68900P9.
  3. For the Cortex Screw Tap, look for Part Number 03.424.126-US, GTIN 10886982335951, and Lot Number 68982P8.
  4. Stop using the recalled device immediately.
  5. Contact Synthes (USA) Products LLC or your distributor to arrange for a return, replacement, or correction of the swapped lots.
  6. Call the FDA Consumer Complaint hotline at 1-888-463-6332 for additional information regarding this recall.

Your Remedy Options

๐Ÿ“‹Other Action
How to: Stop using the recalled device. Contact the manufacturer or your distributor to arrange return, replacement, or correction.

Affected Products

Product: 2.4 VOLT TAP LOCKING SCREW TAP TO 90MM
Model / REF:
03.424.124-US
Lot Numbers:
68900P9
GTIN:
10886982335944

Quantity: 77 units

Product: 2.4 VOLT(TM) TAP CORTEX SCREW TO 90MM
Model / REF:
03.424.126-US
Lot Numbers:
68982P8
GTIN:
10886982335951

Quantity: 33 units

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 98461
Status: Active
Manufacturer: Synthes (USA) Products LLC
Sold By: Medical distributors; Hospitals
Manufactured In: United States
Units Affected: 2 products (77 units; 33 units)
Distributed To: Arkansas, Arizona, California, Colorado, Florida, Indiana, Louisiana, Maryland, Minnesota, North Carolina, New Jersey, Ohio, Oklahoma, Oregon, Pennsylvania, Tennessee, Texas, Utah, Virginia, Washington, Wisconsin

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.

Find an Attorney

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.