RecallRadar

FDA Drug recall D-1312-2022

Bisacodyl Suppositories, Fast Acting Stimulant Laxative, 100 suppositories per box, 10 mg each, Health Star, NDC 57896-443-01

On 2022-08-17 the FDA classified a Class II recall of Bisacodyl Suppositories, Fast Acting Stimulant Laxative, 100 suppositories per box, 10 mg each, Health Star, NDC 57896-443-01 by Mckesson Medical Surgical Corporate Office, citing CGMP Deviations: products were stored outside the drug label specifications.

Read the official FDA Drug notice

AgencyFDA Drug
Recall numberD-1312-2022
ClassificationClass II
Statusterminated
Initiated2022-06-29
Published2022-08-17
Last updated2026-09-13 11:52 UTC
CompanyMckesson Medical Surgical Corporate Office
DistributionUS

Product

Bisacodyl Suppositories, Fast Acting Stimulant Laxative, 100 suppositories per box, 10 mg each, Health Star, NDC 57896-443-01.

Reason

CGMP Deviations: products were stored outside the drug label specifications.

Identifiers

ndc57896-443-66
ndc57896-443-12
ndc57896-443-55
ndc57896-443-05
ndc57896-443-01
code_infoPart# 444-01-HST

Status history

No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:52 UTC. Current status: terminated.

Source

Official record: https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-1312-2022%22

RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.