Stryker Sustainability Solutions 2023-05-24 Health serious FDA
Health · FDA · Recall #FDA-Z-1612-2023
REF 5065, Kendall, Impad Rigid Sole Foot Cover, Regular Pair ,<12", Rx Only Non-Sterile Recall
Issued May 24, 2023 · Stryker Sustainability Solutions
In May 2023, Stryker Sustainability Solutions recalled the REF 5065, Kendall, Impad Rigid Sole Foot Cover, Regular Pair ,<12", Rx Only Non-Sterile, a serious health recall reported by the FDA.
Compiled by Maya Ellison, RecallCheckr
What this means for you
Through complaint surveillance, it was identified that reprocessed Deep vein thrombosis (DVT) Compression Sleeves may be mislabeled and/or mispackaged.
What you should do
- 1 Stop using REF 5065, Kendall, Impad Rigid Sole Foot Cover, Regular Pair ,<12", Rx Only Non-Sterile 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
- May 24, 2023
- Units affected
- Not reported
- Sold at
- US: WA OUS: None
- Recall number
- FDA-Z-1612-2023
- 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 903rd Health recall we've logged in 2023.