FDA Drug Recalls

Recalls / Class II

Class IID-0157-2017

Product

URAMIT MB URINARY ANTISEPTIC Capsules, Each capsule contains: Methenamine 118 mg, Monobasic Sodium Phosphate 40.8 mg, Phenyl Salicylate 36 mg, Methylene Blue 10 mg, Hyoscyamine Sulfate, 0.12 mg, 100 count bottles, Rx only, Manufactured for: BUREL PHARMACEUTICALS, Richland, MS --- NDC 35573-300-10

Affected lot / code info
LOT # 28751601, exp 8/18

Why it was recalled

CGMP Deviations; deficiencies at the manufacturer may result in assay or content uniformity failures

Recalling firm

Firm
Burel Pharmaceuticals Inc
Notification channel
E-Mail
Type
Voluntary: Firm initiated
Address
199 Interstate Dr Ste N, Richland, Mississippi 39218-9433

Distribution

Quantity
2,771 bottles
Distribution pattern
Nationwide

Timeline

Recall initiated
2016-10-24
FDA classified
2016-11-29
Posted by FDA
2016-12-07
Terminated
2017-08-14
Status
Terminated

Source: openFDA Drug Enforcement endpoint. Recall record D-0157-2017. The FDA issues recall classifications as health-hazard assessments, not legal findings; for legal claims consult a licensed attorney.

Class II recall: drug · FDA Drug Recalls