Cardinal Health recalls Diamond Spacer with Large Mask (Item 4742326) due to temperature exposure during shipping, which may cause inaccurate results. Affected units shipped between Feb 23, 2021 and March 10, 2021.
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 Diamond Spacer with Large Mask units that were shipped between February 23, 2021 and March 10, 2021. These units may have been exposed to temperature extremes during shipping, potentially causing inaccurate results.
The devices were exposed to temperature excursions of 31.9°F for up to 2 hours and 15 minutes during shipping. This exposure may cause inaccurate results from the device, but does not pose a direct safety risk to users.
Patients using this medical device for breathing support may be affected. Those who purchased the product between February 23, 2021 and March 10, 2021 are most at risk.
Check for the item number 4742326 on the product label. The product was shipped between February 23, 2021 and March 10, 2021. Look for the NDC/UPC code 8373982700.
Look for the item number 4742326 on the product label to confirm if it's affected.
The devices were exposed to temperature excursions of 31.9°F for up to 2 hours and 15 minutes during shipping, which may cause inaccurate results.
The recall record does not specify a remedy, so no action is required beyond checking if your product is affected.
The product was shipped between February 23, 2021 and March 10, 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-1941-2021 — Cardinal Health Cardinal Health Hello, I own a Cardinal Health that is covered by recall Z-1941-2021 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.
