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DeRoyal Industries Inc recalls DeRoyal Heart Cath Procedure Pack, REF 89-6556.08
Recalled June 16, 2021 · FDA recall Z-1833-2021 · DeRoyal Industries
Hazard
DeRoyal manufactured certain lots of surgical procedure pack products using Hospira Pfizer 1% Lidocaine which was subsequently recalled due to mislabeling; the product is 0.5% Bupivacaine · FDA Class I
Units
66 packs
Sold at
US Nationwide distribution to the states of MS, VA, LA, and NY.
Description
DeRoyal manufactured certain lots of surgical procedure pack products using Hospira Pfizer 1% Lidocaine which was subsequently recalled due to mislabeling; the product is 0.5% Bupivacaine
Product
DeRoyal Heart Cath Procedure Pack, REF 89-6556.08
Manufacturer(s)
DeRoyal Industries Inc
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →