Medline recalls dental procedure kits with model DYNJ909211A that may have slight dimensional variations causing difficulty fitting into outer canister. Affected units include specific lot numbers and serial codes.
A slight dimensional variation which has the potential for increased difficulty fitting into outer canister.
Medline is recalling dental procedure kits labeled DYNJ909211A due to a slight dimensional variation that might make it harder to fit the kit into its outer canister. This issue doesn't pose a safety risk but could cause frustration during use.
The kits have a slight dimensional variation that might cause them to not fit properly into their outer canister. This could lead to difficulty in assembling the kit during dental procedures, but it does not involve physical harm or injury.
Dental professionals and healthcare workers using Medline dental procedure kits with model DYNJ909211A and specific lot numbers (23IBU257, 23KBR755) are likely affected. Those handling the kits daily face the highest risk of fitting issues.
Check for dental procedure kits labeled 'DENTAL, REF DYNJ909211A' with specific lot numbers: 23IBU257 or 23KBR755. The kits also have unique serial numbers: 40195327493234 (case) and 10195327493233 (unit).
Look for the label 'DENTAL, REF DYNJ909211A' and specific lot numbers 23IBU257 or 23KBR755 on the kit.
No, the recall does not require stopping use. The issue is a minor fit problem that doesn't pose a safety risk.
The recall does not include a remedy, so no action is needed beyond checking the label for affected units.
Yes, affected kits have lot numbers 23IBU257 or 23KBR755 with serial numbers 40195327493234 (case) and 10195327493233 (unit).
We’ve drafted a message you can send Medline to request your refund or repair — edit it as you like.
Subject: Recall Z-2702-2024 — Medline Medline Hello, I own a Medline that is covered by recall Z-2702-2024 from Medline. 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.
