KNEE ARTHROSCOPY PK 4/CS Used by medical staff to perform surgical procedures and patient care procedures such as wound healing, suture removals, irrigate wounds, etc. .
Class I - DangerousWhat Should You Do?
- Check if you have this product: Code:9002123 Lots: 141015700 exp. 2/28/16 141216296 exp. 12/31/15 150116519 exp. 1/31/16 150217384 exp. 2/28/16 150317796 exp. 3/31/16 150318119 exp. 4/30/16 150318120 exp. 5/31/16 150418346 exp. 5/31/16 150619248 exp. 6/30/16
- 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.
⚠️ Emergency: If you experience severe symptoms after consuming this product, call 911 or Poison Control at 1-800-222-1222.
Recall Details
- Company:
- Customed, Inc
- Reason for Recall:
- Recall initiated due to inadequate validation/qualification of sterilization processes, and package integrity for products released for distribution as sterile.
- Classification:
- Class I - Dangerous
Dangerous or defective products that predictably could cause serious health problems or death.
- Status:
- terminated
Product Information
Full Description:
KNEE ARTHROSCOPY PK 4/CS Used by medical staff to perform surgical procedures and patient care procedures such as wound healing, suture removals, irrigate wounds, etc. .
Product Codes/Lot Numbers:
Code:9002123 Lots: 141015700 exp. 2/28/16 141216296 exp. 12/31/15 150116519 exp. 1/31/16 150217384 exp. 2/28/16 150317796 exp. 3/31/16 150318119 exp. 4/30/16 150318120 exp. 5/31/16 150418346 exp. 5/31/16 150619248 exp. 6/30/16
Official Source
Always verify recall information with the official FDA source:
View on FDA.govFDA Recall Number: Z-2623-2015
Related Recalls
Recall initiated due to inadequate validation/qualification of sterilization processes, and package integrity for products released for distribution as sterile.
Recall initiated due to inadequate validation/qualification of sterilization processes, and package integrity for products released for distribution as sterile.
Recall initiated due to inadequate validation/qualification of sterilization processes, and package integrity for products released for distribution as sterile.