Applied Medical Resources recalls Epix Universal Clip Appliers with REF: CA500 that may not load clip after trigger actuation. Affected units include specific lot codes. Stop using immediately to prevent potential malfunction.
Their is the potential that Universal Clip applier may not load clip after the trigger is actuated.
Applied Medical Resources is recalling Epix Universal Clip Appliers with REF: CA500 model due to a potential issue where the clip may not load after the trigger is pressed. This could lead to improper use of medical devices, especially for patients needing precise applications.
The clip may not load properly after the trigger is actuated, which could lead to improper application of medical clips. This might cause the device to malfunction during critical procedures, potentially affecting patient safety.
Patients using this clip applier for medical procedures, particularly those requiring precise application of clips. Healthcare providers and medical facilities that use this device are most at risk.
Check for the REF: CA500 model with specific lot codes listed in the recall notice. The product is sold as a sterile medical device for use in healthcare settings.
The recall states that the clip may not load after trigger actuation, so stop using the device to prevent potential malfunction.
The Epix Universal Clip Applier with REF: CA500 is affected by this recall.
Check the lot codes listed in the recall notice, which include specific numbers like 1475580 through 1495845.
The recall does not mention any remedy or fix; the device must be stopped from use immediately.
We’ve drafted a message you can send Applied Medical Resources to request your refund or repair — edit it as you like.
Subject: Recall Z-1388-2024 — Applied Medical Resources Applied Medical Resources Hello, I own a Applied Medical Resources that is covered by recall Z-1388-2024 from Applied Medical Resources. 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.
