Stryker Sustainability Solutions 2024-07-24 Health serious FDA
Health · FDA · Recall #FDA-Z-2405-2024
REF: 60-7070-005, Zimmer, Tourniquet Cuff 30" (Blue), Luer-Lock Dual Port, single… Recall
Issued July 24, 2024 · Stryker Sustainability Solutions
In July 2024, Stryker Sustainability Solutions recalled the REF: 60-7070-005, Zimmer, Tourniquet Cuff 30" (Blue), Luer-Lock Dual Port, single…, a serious health recall reported by the FDA.
Compiled by Maya Ellison, RecallCheckr
What this means for you
Mislabeling; tourniquet cuff packaging labeled as dual port single bladder but contains a tourniquet cuff single port single bladder.
What you should do
- 1 Stop using REF: 60-7070-005, Zimmer, Tourniquet Cuff 30" (Blue), Luer-Lock Dual Port, single… right away.
- 2 Set it aside where it won't be used by mistake.
- 3 Contact Stryker Sustainability Solutions to arrange your voluntary. See the official notice below for contact details.
- 4 Keep the product until your remedy is fully processed. You may need it.
Official remedy (Voluntary):
Recall details
- Brand
- Stryker Sustainability Solutions
- Category
- Health
- Recall date
- July 24, 2024
- Units affected
- Not reported
- Sold at
- US Nationwide distribution in the states of CA, CO, IL, MI, OR, WI.
- Recall number
- FDA-Z-2405-2024
- Made in
- United States
- Issuing agency
- FDA
In context
- Stryker Sustainability Solutions has 6 recalls in our database.
- We're tracking 3,576 Health recalls in our database.
- This is the 737th Health recall we've logged in 2024.