Catalog Number: 9002224 SURGICAL PACK 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: LOTS: SL15177 (150519027) 30-JUN-16 SL15191-01 (150519026) 30-JUN-16 SL15211 (150719756) 31-JUL-16 SL15229 (150820266) 31-AUG-16 SL15258 (150920880) 30-SEP-16 SL15258 (150920802) 30-SEP-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:
Catalog Number: 9002224 SURGICAL PACK 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:
LOTS: SL15177 (150519027) 30-JUN-16 SL15191-01 (150519026) 30-JUN-16 SL15211 (150719756) 31-JUL-16 SL15229 (150820266) 31-AUG-16 SL15258 (150920880) 30-SEP-16 SL15258 (150920802) 30-SEP-16
Official Source
Always verify recall information with the official FDA source:
View on FDA.govFDA Recall Number: Z-1445-2016
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.