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

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.

© 2026 Go Backs. All rights reserved.

Low RiskFDA Device

AAP Implantate Ag: Products were distributed with the incorrect instructions for use.

Agency Publication Date: December 22, 2019
Share:
Sign in to monitor this recall

Affected Products

Product: INTEGRA, Drill CS 4.5, quick coupling single use, REF 430453

Lot Code: QR0013

Lot Numbers:
Code
Product: INTEGRA, Drill CS 4.0, quick coupling single use, REF 430425

Lot Code: QS0007

Lot Numbers:
Code

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 84383
Status: Resolved
Manufacturer: AAP Implantate Ag
Manufactured In: Germany
Units Affected: 2 products (2 units; 7 units)

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 · 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.