Mckesson recalls Ultracell wicks produced between June 1 and September 30, 2021, due to potential temperature excursions 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 recalls Ultracell wicks made between June 1 and September 30, 2021, because they may have been exposed to temperatures that reduced their effectiveness. This could impact medical use if the wicks are part of a critical medical procedure.
The wicks may have been exposed to higher temperatures during shipping or storage between June 2021 and August 2021, which could reduce their effectiveness. This might lead to improper medical outcomes if used in critical procedures.
Healthcare facilities that received these wicks between June 1 and September 30, 2021. Medical staff using these wicks for procedures are at risk if the product's effectiveness is compromised.
Check for the catalog number 30316-C on the product. The wicks were sold between June 1 and September 30, 2021, by Mckesson Medical-Surgical Inc.
Look for the catalog number 30316-C on the wicks to confirm if they were produced between June 1 and September 30, 2021.
The wicks may have been exposed to higher temperatures between June 2021 and August 2021, which could reduce their effectiveness.
Check the catalog number and production dates to see if they fall within the recall period. If so, contact Mckesson for guidance.
The recall is due to potential reduced effectiveness, not immediate safety risks. This could impact medical procedures if the wicks are used in critical applications.
We’ve drafted a message you can send Beaver-Visitec to request your refund or repair — edit it as you like.
Subject: Recall Z-1625-2022 — Beaver-Visitec Beaver-Visitec Hello, I own a Beaver-Visitec that is covered by recall Z-1625-2022 from Beaver-Visitec. 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.
