Kerr Corporation recalls Regimen 28 Day Glutaraldehyde solution due to incorrect immersion time on labels. Product may not sterilize properly if used as instructed.
Immersion time stated on the bottle is 45 minutes while the product instructions say 90 minutes.
Kerr Corporation is recalling Regimen 28 Day Glutaraldehyde Sterilizing Solution because the bottle states 45 minutes immersion time while instructions require 90 minutes. This could lead to improper sterilization of medical instruments.
The product's label shows a 45-minute immersion time, but the instructions specify 90 minutes. Using it for less time may not properly sterilize medical instruments, potentially leading to infection risks.
Healthcare professionals using surgical instruments or medical equipment that require sterilization. Those using the product without following the correct immersion time are at risk of inadequate sterilization.
Check for the product name 'Regimen 28 Day Glutaraldehyde Sterilizing and Disinfecting Solution' with lot numbers listed in the recall: 16 1250, 16 1274, 16 1324A, 16 1324B, 16 2337, 17 1038, 17 1038A, 17 1083, 17 1193, 17 1262, 17 2122, 17 2142, 17 2219, 17 2306, 17 2347A, 18 1092B, 18 1121, 18 2037, and 18 3164.
Look for the lot numbers listed in the recall: 16 1250, 16 1274, 16 1324A, 16 1324B, 16 2337, 17 1038, 17 1038A, 17 1083, 17 1193, 17 1262, 17 2122, 17 2142, 17 2219, 17 2306, 17 2347A, 18 1092B, 18 1121, 18 2037, and 18 3164.
The product's label states a 45-minute immersion time while the instructions require 90 minutes, which could lead to improper sterilization of medical instruments.
Check the product label for the listed lot numbers. If you have the recalled product, you may need to follow the correct immersion time as per the instructions.
The recall record does not mention a remedy or fix for this issue.
We’ve drafted a message you can send Kerr Corporation to request your refund or repair — edit it as you like.
Subject: Recall Z-1721-2019 — Kerr Corporation Kerr Corporation Hello, I own a Kerr Corporation that is covered by recall Z-1721-2019 from Kerr Corporation. 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.
