MPM Medical LLC recalls REGENECARE HA (Lidocaine HCL 2%) Topical Anesthetic Hydrogel, Net Wt. 3 oz. (85 g), Manufactured For: MPM Medical Mesqu
Recalled December 9, 2020 · FDA recall D-0118-2021 · MPM Medical
Hazard
Microbial Contamination of Non-Sterile Drug Product. The product was found to be contaminated with the bacteria Burkholderia cepecia. · FDA Class I
Units
7,637 tubes
Sold at
Distributed Nationwide in the USA
Description
Microbial Contamination of Non-Sterile Drug Product. The product was found to be contaminated with the bacteria Burkholderia cepecia.
Product
REGENECARE HA (Lidocaine HCL 2%) Topical Anesthetic Hydrogel, Net Wt. 3 oz. (85 g), Manufactured For: MPM Medical Mesquite, TX 75149. NDC 66977-107-03
Manufacturer(s)
MPM Medical LLC
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →