Mckesson Medical-Surgical recalls 10gm sensory foot monofilament test strips (model AM140) produced between June 2021 and August 2021 due to potential temperature issues affecting product effectiveness.
Facility Temperature excursions (from June 2021-August 2021) prior to delivery; exposure to higher temperatures may have impacted product effectiveness. All lots received between 06/01/21-9/30/21.
Mckesson Medical-Surgical is recalling a specific type of sensory foot test strips that may have been affected by temperature changes during production. This could impact how well the product works for medical testing purposes.
The product was exposed to higher temperatures during production between June 2021 and August 2021, which may have reduced its effectiveness. This could lead to inaccurate sensory foot testing results if the product does not function as intended.
Healthcare professionals using these test strips for sensory foot assessments may be affected. Patients using these strips for medical testing could be at risk if the product's effectiveness is compromised.
Check for the model number AM140 on the packaging. The product was sold between June 1, 2021, and September 30, 2021.
Verify the production date on the packaging to ensure it falls between June 1, 2021, and September 30, 2021.
The product was exposed to higher temperatures during production between June 2021 and August 2021, which may have impacted its effectiveness.
Look for the model number AM140 on the packaging and check if it was purchased between June 1, 2021, and September 30, 2021.
The recall does not specify a remedy, so you should check with the manufacturer for guidance on whether to use or discard the product.
We’ve drafted a message you can send Mckesson Medical-Surgical to request your refund or repair — edit it as you like.
Subject: Recall Z-1802-2022 — Mckesson Medical-Surgical Mckesson Medical-Surgical Hello, I own a Mckesson Medical-Surgical that is covered by recall Z-1802-2022 from Mckesson Medical-Surgical. 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.
