Aircast REF 3011 - PL RX only VF-PL Sterile Cuff Pkg., Lot# 418003, Expiration Date: 2020 -12 - 31, Made in Mexico, DJO, LLC.
Class I - DangerousWhat Should You Do?
- Check if you have this product: Lot # 418003 UDI: (01)00888912302418
- 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:
- DJO, LLC
- Reason for Recall:
- The product may not meet sterility requirements. Product labeled as sterile, however all units do not appear to meet sterility requirements.
- Classification:
- Class I - Dangerous
Dangerous or defective products that predictably could cause serious health problems or death.
- Status:
- ongoing
Product Information
Full Description:
Aircast REF 3011 - PL RX only VF-PL Sterile Cuff Pkg., Lot# 418003, Expiration Date: 2020 -12 - 31, Made in Mexico, DJO, LLC.
Product Codes/Lot Numbers:
Lot # 418003 UDI: (01)00888912302418
Official Source
Always verify recall information with the official FDA source:
View on FDA.govFDA Recall Number: Z-1985-2019
Related Recalls
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Due to broken connector which may result in a temporary interruption of prescribed cold therapy.
The IFU (Information for Use) on the wrap instructs the user to heat the hot and cold compression wrap in the microwave for 3 minutes, which may cause the wrap to leak or break at the seams and/or reach temperatures capable of causing a second degree burn.