BD recalls 100 NANO UF PENs shipped between Feb 2020 and March 2021 due to temperature exposure potentially causing inaccurate test results. Consumers should check lot numbers for affected units.
Due to shipping delays the devices were exposed to temperature excursions of 31.9¿F, intermittently over a 2 hour and 15 minute period of time which may cause inaccurate results.
BD is recalling 100 NANO UF PENs that were shipped between February 2020 and March 2021 because they may have been exposed to temperature extremes during shipping, which could lead to inaccurate test results. This recall affects users who rely on these devices for medical testing.
The devices were exposed to temperature excursions of 31.9°F over a 2 hour and 15 minute period during shipping. This temperature change may cause the devices to produce inaccurate test results when used.
Users of BD UF PEN 32GX4MM 100 NANO devices who purchased them between February 2020 and March 2021 are likely affected. Those using these devices for medical testing are at the highest risk of inaccurate results.
Check the lot numbers on the device packaging, which were shipped between February 2020 and March 2021. The product has a specific item number: 4292272 and NDC/UPC: 8290320122.
Look for the lot number on the device packaging, which was shipped between February 2020 and March 2021.
The devices were exposed to temperature excursions of 31.9°F over a 2 hour and 15 minute period during shipping, which may cause inaccurate test results.
Check the lot numbers on the device packaging, which were shipped between February 2020 and March 2021. The product has a specific item number: 4292272 and NDC/UPC: 8290320122.
The recall record does not specify any remedy steps for this product.
We’ve drafted a message you can send BD to request your refund or repair — edit it as you like.
Subject: Recall Z-1933-2021 — BD BD Hello, I own a BD that is covered by recall Z-1933-2021 from BD. 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.
