Aesculap recalls MB215R micro needle holders distributed as MB362R between Nov 2022 and Oct 2023 due to potential procedure delays.
Needle Holder MB215R was inadvertently distributed as MB362R. Similarly, MB362R was distributed as MB215R during the affected distribution date range. The issue may lead to a short delay in procedure.
Aesculap is recalling MB215R micro needle holders that were mistakenly distributed as MB362R. This could cause short delays in medical procedures if used without correction.
The MB215R model was accidentally distributed as MB362R and vice versa during the affected time frame. This mix-up could cause temporary delays in surgical procedures if the wrong model is used.
Surgical staff using the MB215R micro needle holders during the distribution period (Nov 2022 - Oct 2023) are most at risk. Patients undergoing procedures with these tools may experience brief delays.
Check for the model number 'MB215R' on the product label. The affected items were distributed between November 23, 2022 and October 6, 2023. The product description includes 'TC MILLS NDLE HOLDRRND HNDLSTR203MM'.
Look for the model number 'MB215R' on the product label to confirm if it's affected.
The MB215R model was inadvertently distributed as MB362R and vice versa during the affected distribution period, which could cause short delays in procedures.
The official recall notice does not specify a remedy or action for affected products.
The affected product was distributed between November 23, 2022 and October 6, 2023.
We’ve drafted a message you can send Aesculap to request your refund or repair — edit it as you like.
Subject: Recall Z-0867-2024 — Aesculap Aesculap Hello, I own a Aesculap that is covered by recall Z-0867-2024 from Aesculap. 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.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
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.
