Argon Medical Devices recalls SuperCore biopsy instruments with serial numbers listed. Component detachment could cause injury during medical procedures.
Due to component (housing and plunger) detaching from the semi-automatic biopsy instruments.
Argon Medical Devices is recalling SuperCore biopsy instruments due to a risk that the housing or plunger may detach during use. This could lead to injury if the instrument is used improperly.
The housing and plunger components can detach from the biopsy instruments during use. This detachment could cause injury if the instrument is not securely attached and used correctly during medical procedures.
Medical professionals who own or use the recalled SuperCore biopsy instruments are affected. Those using the instruments for procedures without proper attachment are at higher risk.
Check for the product model numbers listed in the recall: 701114090, 701114150, 701116090, 701118060, 701118090, 701118150, 701118200, 701120090, 701120150, 701120200, 701214090, 701214150, 701216090, 701216150, 701218090, 701218150, 701218200, 701220090, 701220150, 701220200, 701114090M, 701114150M, 701116090M, SC 1409/PGI Supercore, SC 1609/PGI Supercore, SC 1806/PGI Supercore. Also check the lot numbers provided in the recall notice.
Identify your instrument's model number and lot number to confirm if it is recalled.
Reach out to Argon Medical Devices for guidance on the recall process and necessary actions.
The recalled models include 701114090, 701114150, 701116090, 701118060, 701118090, 701118150, 701118200, 701120090, 701120150, 701120200, 701214090, 701214150, 701216090, 701216150, 701218090, 701218150, 701218200, 701220090, 701220150, 701220200, 701114090M, 701114150M, 701116090M, SC 1409/PGI Supercore, SC 1609/PGI Supercore, and SC 1806/PGI Supercore.
Check the model number and lot number on your instrument against the list provided in the recall notice.
Contact Argon Medical Devices for instructions on how to handle the recalled instrument.
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-0354-2022 — Argon Medical Devices Argon Medical Devices Hello, I own a Argon Medical Devices that is covered by recall Z-0354-2022 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.
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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.
