HEALICOIL RG SA 5.5MM W/3 UB-BL CB BL BK- Absorbable Suture anchor Product Number: 72203707
Class I - DangerousWhat Should You Do?
- Check if you have this product: Batch Numbers: 2011426 2011425 2011427 2014000 2014001 2016191 2016231 2016190 2017773 2017813 2017845 2018741 2018798 2018852 2019891 2019890 2020050 2021455 2021497 2021545 2023183 2023182 2023271 2024718 2024720 2024722 2027219 2027436 2027406 2029150 2029352 2029399 2030953 2030954 2031092 2031093 2031157 2031158 2032824 2032825 2033399 2033398 2033538 2033537 2035454 2035455 2035540 2035541 2036290 2036696 2037152 2038469 2038804 2038805 2039452 2039453 2039454 2039455 2041421 2041071 2041072 2041073 2041074 2042598 2042779 2042778 2045871 2045872 2045873 2045874 2045875 2044895 2046745 2048396 2048397 2048398 2048401 2048402 2048403 2049922 2049923 2049917 2049918 2048399 2049919 2049920 2049921 2051017 2051018 2051019 2052178 2052181 2052179 2052180 2052182 2052183 2053917 2053918 2053919 2053920 2056083 2053915 2056082 2048400 2056429 2056430 2056431 2057399 2057400 2057401
- 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:
HEALICOIL RG SA 5.5MM W/3 UB-BL CB BL BK- Absorbable Suture anchor Product Number: 72203707
Product Codes/Lot Numbers:
Batch Numbers: 2011426 2011425 2011427 2014000 2014001 2016191 2016231 2016190 2017773 2017813 2017845 2018741 2018798 2018852 2019891 2019890 2020050 2021455 2021497 2021545 2023183 2023182 2023271 2024718 2024720 2024722 2027219 2027436 2027406 2029150 2029352 2029399 2030953 2030954 2031092 2031093 2031157 2031158 2032824 2032825 2033399 2033398 2033538 2033537 2035454 2035455 2035540 2035541 2036290 2036696 2037152 2038469 2038804 2038805 2039452 2039453 2039454 2039455 2041421 2041071 2041072 2041073 2041074 2042598 2042779 2042778 2045871 2045872 2045873 2045874 2045875 2044895 2046745 2048396 2048397 2048398 2048401 2048402 2048403 2049922 2049923 2049917 2049918 2048399 2049919 2049920 2049921 2051017 2051018 2051019 2052178 2052181 2052179 2052180 2052182 2052183 2053917 2053918 2053919 2053920 2056083 2053915 2056082 2048400 2056429 2056430 2056431 2057399 2057400 2057401
Official Source
Always verify recall information with the official FDA source:
View on FDA.govFDA Recall Number: Z-0171-2021
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.