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SunMed Holdings, LLC recalls Full Kit Pulset 3cc Syringe 23g x 1 Safety Tip 25u BH, REF Number 3373-91
Recalled October 5, 2022 · FDA recall Z-1779-2022 · SunMed Holdings
Hazard
The kits are being recalled due to a lack of sterility of a spare needle contained within the kits. There is a potential for skin infection or sepsis if the patient is exposed to a non-sterilized, unused needle. · FDA Class II
Units
53,560 units
Sold at
Domestic distribution to AL, FL, GA, IL, LA, MO, NJ, NY, TN, TX.
Description
The kits are being recalled due to a lack of sterility of a spare needle contained within the kits. There is a potential for skin infection or sepsis if the patient is exposed to a non-sterilized, unused needle.
Product
Full Kit Pulset 3cc Syringe 23g x 1 Safety Tip 25u BH, REF Number 3373-91
Manufacturer(s)
SunMed Holdings, LLC
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →