Cardinal Health recalls ONETOUCH DELICA LANCETS 33G 100 COUNT (item 5541628) sold between Feb 2020 and March 2021 due to potential inaccurate blood test results from temperature exposure during shipping.
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 33G lancets for blood glucose testing that may give inaccurate results because they were exposed to cold temperatures during shipping. This could lead to incorrect blood sugar readings if used.
The lancets were exposed to cold temperatures (31.9°F) during shipping for over two hours, which may cause the devices to give inaccurate blood test results. This could lead to incorrect blood sugar readings if the lancets are used.
People who own or use the ONETOUCH DELICA LANCETS 33G 100 COUNT (item 5541628) sold between February 2020 and March 2021 are affected. Those who test blood glucose frequently are most at risk of inaccurate results.
Check for the ONETOUCH DELICA LANCETS 33G 100 COUNT with item number 5541628. They were sold between February 2020 and March 2021.
Verify if your lancets have the item number 5541628 and were sold between February 2020 and March 2021.
The lancets were exposed to cold temperatures (31.9°F) during shipping for over two hours, which may cause inaccurate blood test results.
No, but you should check if your lancets were affected by the temperature exposure and verify the item number and sale dates.
Check for the ONETOUCH DELICA LANCETS 33G 100 COUNT with item number 5541628 sold between February 2020 and March 2021.
We’ve drafted a message you can send Cardinal Health to request your refund or repair — edit it as you like.
Subject: Recall Z-1940-2021 — Cardinal Health Cardinal Health Hello, I own a Cardinal Health that is covered by recall Z-1940-2021 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.
