Cardinal Health recalls 30G 100-count lancets from 2/23/2020 to 3/10/2021 due to temperature exposure causing inaccurate blood test results. Consumers should check lot numbers and contact the company for details.
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.
Cardinal Health is recalling 30G 100-count ONETOUCH DELICA LANCETS that were shipped between February 23, 2020 and March 10, 2021. These lancets may give inaccurate blood test results because they were exposed to temperature extremes during shipping.
The lancets were exposed to temperature extremes during shipping, which can cause them to give inaccurate blood test results. This means blood glucose readings might be too high or too low, but it does not cause physical harm.
People who own or use the recalled lancets, particularly those who test blood glucose regularly. The risk is low as the issue is related to inaccurate results, not injury.
Check the lot numbers on the lancet packaging, which were shipped between February 23, 2020 and March 10, 2021. The product is labeled as ONETOUCH DELICA LANCETS 30G 100 COUNT with item number 5541610.
Look for lot numbers on the lancet packaging that were shipped between February 23, 2020 and March 10, 2021.
The lancets were exposed to temperature extremes during shipping, which may cause inaccurate blood test results.
Check the lot numbers on the packaging, which were shipped between February 23, 2020 and March 10, 2021.
No, but you should check if your lancets are in the recalled batch and consider using a different brand if results are inconsistent.
We’ve drafted a message you can send Cardinal Health to request your refund or repair — edit it as you like.
Subject: Recall Z-1939-2021 — Cardinal Health Cardinal Health Hello, I own a Cardinal Health that is covered by recall Z-1939-2021 from Cardinal Health. 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.
