Argon Medical Devices recalls BioPince Full Core Biopsy Instruments due to incorrect labeling. This may cause confusion in medical use. Consumers should contact the manufacturer for details.
Incorrect product labeling.
Argon Medical Devices is recalling BioP: Full Core Biopsy Instruments with incorrect labeling. This could lead to confusion in medical procedures, potentially affecting patient safety.
Incorrect labeling could cause confusion about the product's specifications, potentially leading to improper use in medical procedures. However, the hazard does not involve immediate physical harm or serious injury.
Medical professionals who use the BioPince instruments for biopsies may be affected. Patients using these instruments are at low risk due to the labeling issue.
Check for the model number 370-1580-01 and the lot number 11277175 on the BioPince Full Core Biopsy Instrument. The product is sold in packs of 5.
Verify the model number (370-1580-01) and lot number (11277175) on the instrument.
No, the recall is due to incorrect labeling, not a safety hazard. The product is safe for use but needs proper identification.
Look for the model number 370-1580-01 and lot number 11277175 on the BioPince Full Core Biopsy Instrument.
Check the labeling to confirm the model and lot numbers. Contact Argon Medical Devices for further instructions.
We’ve drafted a message you can send Argon Medical Devices to request your refund or repair — edit it as you like.
Subject: Recall Z-2427-2020 — Argon Medical Devices Argon Medical Devices Hello, I own a Argon Medical Devices that is covered by recall Z-2427-2020 from Argon Medical Devices. 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.
