Barricaid Annular Closure Impactor, REF: BAR-IMPACTOR, P/N: 400906-A
Class I - Dangerous ๐ฅ Medical Devices
Recalled: July 25, 2024 Intrinsic Therapeutics Other Medical Devices
Nationwide
What Should You Do?
- Check if you have this product: REF: BAR-IMPACTOR, P/N: 400906-A; UDI-DI: M906IMP1A0; Lot numbers: 10282203, 06152307, 08292301, 10112307.
- Do not eat it: Even if it looks and smells fine, do not consume this product.
- Throw it away or return it: You can return the product to the store for a full refund.
- Seek medical attention if needed: If you've consumed this product and feel unwell, contact your doctor immediately.
- Report problems: Report any issues to the FDA's Safety Reporting Portal.
โ ๏ธ Emergency: If you experience severe symptoms after consuming this product, call 911 or Poison Control at 1-800-222-1222.
Recall Details
- Company:
- Intrinsic Therapeutics, Inc.
- Reason for Recall:
- At least two units have been found to be missing a weld.
- Classification:
- Class I - Dangerous
Dangerous or defective products that predictably could cause serious health problems or death.
- Status:
- ongoing
Product Information
Full Description:
Barricaid Annular Closure Impactor, REF: BAR-IMPACTOR, P/N: 400906-A
Product Codes/Lot Numbers:
REF: BAR-IMPACTOR, P/N: 400906-A; UDI-DI: M906IMP1A0; Lot numbers: 10282203, 06152307, 08292301, 10112307.
Official Source
Always verify recall information with the official FDA source:
View on FDA.govFDA Recall Number: Z-2688-2024
Related Recalls
The catalog ( REF ) number on the peelable inner labels (patient sticker) that is on the inner container (box) is incorrect. It states BAR-A8-10MM instead of BAR-A8-8MM.