McKesson recalls certain fertility and pregnancy test kits from June 2021 to September 2021 that may have been affected by temperature excursions, potentially reducing 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 specific fertility and pregnancy test kits produced between June 1 and September 30, 2021. These kits may have been impacted by temperature changes during shipping, which could reduce their effectiveness. Affected kits were sold with model numbers 5000, 5001, and 5002.
The test kits were exposed to higher temperatures during shipping from June 2021 to August 2021, which could have reduced their effectiveness. This means the results might not be accurate if the kits were used after being affected by temperature changes.
Pregnancy and fertility test kit users who purchased the recalled models between June 1 and September 30, 2021. Those who used the kits after the recall period may not be affected.
Check for model numbers 5000, 5001, or 5002 on the packaging. The kits were sold between June 1 and September 30, 2021, with specific GTINs listed in the recall notice.
Look for model numbers 5000, 5001, or 5002 on the test kit packaging.
The recall indicates potential reduced effectiveness due to temperature exposure, but the kits may still be safe to use if not affected by temperature changes.
The recall does not specify a return process, so no action is required beyond checking if the kit is affected.
The kits were produced and shipped between June 1 and September 30, 2021.
We’ve drafted a message you can send McKesson to request your refund or repair — edit it as you like.
Subject: Recall Z-1587-2022 — McKesson McKesson Hello, I own a McKesson that is covered by recall Z-1587-2022 from McKesson. 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.
