DONJOY Ultrasing Pro arm slings with failed rivets at the chafe tab may cause injury during medical use. Recalled for safety due to potential failure in intended medical applications.
failed rivet at the chafe tab of arm sling.
DONJOY Ultrasing Pro arm slings intended for medical use have a failed rivet at the chafe tab that could cause injury. This recall affects specific production lots from November 2020 through March 2021.
The rivet at the chafe tab can fail under normal use, potentially causing the sling to break or slip. This could lead to injury if the arm is immobilized improperly.
People using this medical arm sling for immobilization are affected. Those with medical conditions requiring arm support are at higher risk.
Check for the product name 'Ultrasing Pro' with the lot numbers listed from November 2020 through March 2021. The item is intended for medical use only.
Look for the lot numbers listed in the recall: 2020-11-17 through 2021-03-19.
If you have the recalled model, stop using it now to prevent potential injury.
The recall indicates a risk of injury due to a failed rivet. Do not use the recalled model until you confirm it's not affected.
The recall does not specify a remedy. Check the lot numbers to see if your product is affected and stop using it if it is.
Check for the lot numbers listed: 2020-11-17 through 2021-03-19. The product is intended for medical use only.
We’ve drafted a message you can send DONJOY to request your refund or repair — edit it as you like.
Subject: Recall Z-1511-2021 — DONJOY DONJOY Hello, I own a DONJOY that is covered by recall Z-1511-2021 from DONJOY. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.