Mckesson recalls Wetfield Eraser Bipolar Hemostatic Erasers (model 221265) 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 is recalling Wetfield Eraser Bipolar Hemostatic Erasers (model 221265) that were produced between June 1 and August 30, 2021. The recall is because these erasers may have been exposed to temperatures that could reduce their effectiveness during use.
The erasers were produced during a period when facility temperatures may have fluctuated. These temperature changes could potentially reduce the eraser's effectiveness in controlling bleeding during medical procedures.
Healthcare facilities that purchased Wetfield Erasers with model number 221265 between June 1 and August 30, 2021. Medical professionals using these erasers for hemostasis are most at risk.
Check for model number 221265 on the eraser. The recall covers units purchased between June 1 and August 30, 2021.
Verify the model number on the eraser to confirm it is 221265.
Reach out to Mckesson Medical-Surgical for guidance on next steps.
The erasers may have been exposed to temperature fluctuations between June 1 and August 30, 2021, which could reduce their effectiveness.
Look for model number 221265 on the eraser, and check if it was purchased between June 1 and August 30, 2021.
Contact Mckesson Medical-Surgical for guidance on next steps.
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-1594-2022 — Mckesson Medical-Surgical Mckesson Medical-Surgical Hello, I own a Mckesson Medical-Surgical that is covered by recall Z-1594-2022 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.
