Acumed LLC 2024-01-03 Health serious FDA
Health · FDA · Recall #FDA-Z-0618-2024
RibLoc U Plus 90 Instrument PRIMARY GUIDE ASSY, LOW PROFILE REF RBL2320 The RBL2320,… Recall
Issued January 3, 2024 · Acumed LLC
In January 2024, Acumed LLC recalled the RibLoc U Plus 90 Instrument PRIMARY GUIDE ASSY, LOW PROFILE REF RBL2320 The RBL2320,…, a serious health recall reported by the FDA.
Compiled by Maya Ellison, RecallCheckr
What this means for you
Due to potential breakage during use.
What you should do
- 1 Stop using RibLoc U Plus 90 Instrument PRIMARY GUIDE ASSY, LOW PROFILE REF RBL2320 The RBL2320,… right away.
- 2 Set it aside where it won't be used by mistake.
- 3 Contact Acumed LLC 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
- Acumed LLC
- Category
- Health
- Recall date
- January 3, 2024
- Units affected
- Not reported
- Sold at
- Worldwide - U.S. Nationwide distribution including in the states of AL, AZ, CA, CO, FL, GA, ID, IL, IN, KS, LA, MA, MD, MI, MN, MO, NC, NJ,
- Recall number
- FDA-Z-0618-2024
- Made in
- United States
- Issuing agency
- FDA
In context
- Acumed LLC has 1 recall in our database.
- We're tracking 3,576 Health recalls in our database.
- This is the 737th Health recall we've logged in 2024.