Independent register of U.S. FDA drug recalls · updated Oct 10, 2026
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Class II · Moderate risk Terminated Initiated Jul 11, 2019 (7 years ago)

Adult Glycerin Suppositories (Glycerin Suppository)

Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.

Why it was recalled

CGMP Deviations: Out of Specification results for either total microbial count or total organic carbon in the purified water utilized in the manufacturing process.

Cause type: Microbial contamination

Bacteria, mold, yeast or other microorganisms detected in the product. Contamination can occur from water systems, equipment or handling, and can cause infection. All microbial contamination recalls.

What was recalled

Adult Glycerin Suppositories, Package Size 25-count suppositories, Distributed By: Walgreen Co. 200 Wilmot Rd. Deerfield, IL 60015. NDC#0363-0445-25,

Affected NDC 0363-0445-25

Compare with the code on your package — it is the most precise check available.

Product details

From the FDA NDC directory, for the product code this recall names. Compare with the label on your package.

ProductStrengthForm & routeLabelerType
Walgreens Adult Glycerin Laxative
Glycerin Suppository
NDC 00363-0445
GLYCERIN 2 g/1 Suppository
Rectal
Walgreens OTC
Recalling firm
US Pharmaceuticals Inc.
NDC code
0363-0445-25
Origin
NJ, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-1728-2019 · FDA notice

Check, then ask. Class II means harm is possible but usually temporary or reversible. Find the lot number on your package; if it matches, ask your pharmacist about a replacement. Do not simply stop a prescribed medication on your own - the gap can be riskier than the recall. This recall is now terminated, which means the firm has finished removing the affected product; anything on pharmacy shelves today should be unaffected.

Other recalls by US Pharmaceuticals Inc.

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Kool Comfort Cooling Pain Relief

CGMP Deviations: Out of Specification results for either total microbial count or total organic carbon in the purified water utilized in the manufacturing process.

Terminated Microbial contamination US Pharmaceuticals Inc. D-1739-2019

Other microbial contamination recalls from 2019

All microbial contamination recalls