Recall of Medical Action Industries Minor Procedure Tray (REF 61214) due to potential flaking metal and brown spots on hemostats. Affected units have specific batch numbers and expiration dates.
There is a potential for flaking metal and/or brown spots on the hemostats sold as individual units or packaged in the kits
Medical Action Industries is recalling its Minor Procedure Tray (REF 61214) because some units may have flaking metal or brown spots on the hemostats. This could cause injury during medical procedures if the metal flakes off and enters the patient.
The hemostats (surgical clamps) in the tray may develop flaking metal or brown spots due to manufacturing defects. If metal flakes off during use, it could potentially enter the patient's body and cause injury.
Medical professionals using the Minor Procedure Tray for minor procedures are most at risk. Patients undergoing procedures with this tray could be affected if metal flakes cause injury.
Check for batch numbers 0000275137 (expiring May 29, 2022) or 0000276914 (expiring February 1, 2023) on the tray packaging. The product is sold under the brand name Medical Action Industries.
Look for batch numbers 0000275137 (expiring May 29, 2022) or 0000276914 (expiring February 1, 2023) on the tray packaging.
The recall is due to potential flaking metal and brown spots on the hemostats, which could cause injury if metal flakes enter the patient during use.
Check the batch numbers on the packaging. If you have batch numbers 0000275137 (expiring May 29, 2022) or 0000276914 (expiring February 1, 2023), contact Medical Action Industries for instructions.
The recall states potential flaking metal and brown spots, but no specific mention of serious injury. The danger level is low risk.
We’ve drafted a message you can send Medical Action Industries to request your refund or repair — edit it as you like.
Subject: Recall Z-1949-2021 — Medical Action Industries Medical Action Industries Hello, I own a Medical Action Industries that is covered by recall Z-1949-2021 from Medical Action Industries. 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.
