OSTEORAPTOR 2.9 W/ 2 UB WHITE / BLUE -Absorbable Suture anchor Product Number: 72201995
Class I - DangerousWhat Should You Do?
- Check if you have this product: Batch Numbers: 2012909 2012911 2012910 2012937 2013912 2013913 2016202 2016230 2016203 2018636 2018637 2018740 2018795 2021326 2022258 2023091 2024440 2024441 2024439 2024448 2024449 2025098 2025094 2025340 2025287 2027419 2027388 2025288 2027453 2029073 2027483 2029325 2029326 2029366 2029365 2030990 2030989 2031123 2031125 2031127 2032788 2033240 2033239 2033375 2033376 2033497 2034385 2034386 2034387 2034458 2034459 2035471 2035472 2035473 2035521 2035522 2035523 2035524 2035526 2035525 2036692 2039227 2039228 2039424 2039584 2039585 2040072 2040706 2040708 2040709 2042563 2042564 2042565 2042745 2042746 2044792 2044794 2044795 2044796 2044797 2044793 2045742 2045743 2045744 2045745 2045746 2046744 2048188 2048189 2048190 2048191 2048192 2049661 2049662 2049655 2049656 2049657 2049658 2049660 2049659 2056309 2056311 2056310 2056312 2056313
- 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:
- Smith & Nephew, Inc.
- Reason for Recall:
- Product packaging improper or incomplete seal of the pouch surrounding the sterile product may result in a breach of the sterile barrier created by the pouch
- Classification:
- Class I - Dangerous
Dangerous or defective products that predictably could cause serious health problems or death.
- Status:
- ongoing
Product Information
Full Description:
OSTEORAPTOR 2.9 W/ 2 UB WHITE / BLUE -Absorbable Suture anchor Product Number: 72201995
Product Codes/Lot Numbers:
Batch Numbers: 2012909 2012911 2012910 2012937 2013912 2013913 2016202 2016230 2016203 2018636 2018637 2018740 2018795 2021326 2022258 2023091 2024440 2024441 2024439 2024448 2024449 2025098 2025094 2025340 2025287 2027419 2027388 2025288 2027453 2029073 2027483 2029325 2029326 2029366 2029365 2030990 2030989 2031123 2031125 2031127 2032788 2033240 2033239 2033375 2033376 2033497 2034385 2034386 2034387 2034458 2034459 2035471 2035472 2035473 2035521 2035522 2035523 2035524 2035526 2035525 2036692 2039227 2039228 2039424 2039584 2039585 2040072 2040706 2040708 2040709 2042563 2042564 2042565 2042745 2042746 2044792 2044794 2044795 2044796 2044797 2044793 2045742 2045743 2045744 2045745 2045746 2046744 2048188 2048189 2048190 2048191 2048192 2049661 2049662 2049655 2049656 2049657 2049658 2049660 2049659 2056309 2056311 2056310 2056312 2056313
Official Source
Always verify recall information with the official FDA source:
View on FDA.govFDA Recall Number: Z-0152-2021
Related Recalls
META-TAN LAG/COMPRESSION SCREW KIT 90MM/85MM, REF: 71642690
Smith & Nephew
Integrated Lag/Compression Screw Kit has a compression screw with hexagon socket that may be undersized, which causes the screw to be non-functional, which would require replacement with another adequate size screw, and exchange may exceed 30 minutes.
Sterile barrier breach due to inadequate packaging design that could not hold the geometry of the device.
The Bipolar assembly contains an oversized Retainer Ring.