Miami J Collar Product Usage: Miami J collars are applied to patients afflicted with cervical injuries to ensure immobilization.
Class I - DangerousWhat Should You Do?
- Check if you have this product: Item No: MJ-200B MJ-200L MJ-200LFRT MJ-200S MJ-200SFRT MJ-250 MJ-250FRT MJ-2530 MJ-300 MJ-300FRT MJ-400 MJ-400FRT MJ-500 MJ-500FRT MJ-P2 MJ-P3 MJR-200L MJR-200S MJR-250 MJR-2530 MJR-300 MJR-400 MJR-500 MJR-P2 MJR-P3
- 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:
- Ossur H / F
- Reason for Recall:
- Ossur Americas is recalling , Knee Shield / Patella Cup, Knee Undersleeve Gray, NecLoc Extrication Collar, Rebound Cartilage, Rebound Cartilage Custom, Rebound Air Walker, Rebound Diabetic Walker, Back Support Suspenders Clip on Black, Back Support Suspenders Sew On Black, Extreme Custom, Unloader Custom XT, Unloader Custom Lite, Unloader Custom, and Papoose Infant Spine Immobilizers because the p
- Classification:
- Class I - Dangerous
Dangerous or defective products that predictably could cause serious health problems or death.
- Status:
- terminated
Product Information
Full Description:
Miami J Collar Product Usage: Miami J collars are applied to patients afflicted with cervical injuries to ensure immobilization.
Product Codes/Lot Numbers:
Item No: MJ-200B MJ-200L MJ-200LFRT MJ-200S MJ-200SFRT MJ-250 MJ-250FRT MJ-2530 MJ-300 MJ-300FRT MJ-400 MJ-400FRT MJ-500 MJ-500FRT MJ-P2 MJ-P3 MJR-200L MJR-200S MJR-250 MJR-2530 MJR-300 MJR-400 MJR-500 MJR-P2 MJR-P3
Distribution:
Nationwide distribution
Official Source
Always verify recall information with the official FDA source:
View on FDA.govFDA Recall Number: Z-1288-2016
Related Recalls
Pressure sensitive adhesive hooks attached to the sides of the anterior cervical orthosis collar panel can occasionally exhibit poor adhesion, which may lead to them gradually peeling off with repeated doffing, possibly leading to reduced immobilization of the cervical spine.
Due to firmware issues with the prosthetic knee, there is the potential for unintended warnings and device shutdown which could result in patient falls.
Due to firmware issues with the prosthetic knee, there is the potential for unintended warnings and device shutdown which could result in patient falls.