Class I · High risk
Regenecare Ha
Microbial Contamination of Non-Sterile Drug Product. The product was found to be contaminated with the bacteria Burkholderia cepecia.
National Drug Code
Is NDC 66977-0107-03 recalled?
Regenecare Ha · 85 g in 1 TUBE (66977-107-03)
Yes — this exact package was recalled
1 FDA recall names the code 66977-0107-03 directly. A recall still applies to particular lot numbers — compare the lot on your package with the FDA notice below, and talk to your pharmacist before stopping a prescribed medication.
- Active ingredient
- lidocaine HCl
- Strength
- LIDOCAINE HYDROCHLORIDE 20 mg/g
- Form
- Gel · Topical
- Labeler
- MPM Medical LLC
- Type
- Human OTC Drug
- Product code
- 66977-0107
Recalls naming this package
Where to find this code. The NDC is printed on the pharmacy label and on the manufacturer's carton, usually as three groups of digits after “NDC”. The last group is the package size — two bottles of the same medicine can differ only in that group, and a recall may cover one but not the other.
Free recall alerts
Know the day your medication is recalled
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