Med Pride Bacitracin Zinc Ointment Recall
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Dabur India Limited is recalling 1185 tubes of Med Pride Bacitracin Zinc Ointment due to CGMP deviations observed during an FDA inspection.
What this FDA recall tells you, and what most readers miss
This notice was issued by FDA on August 1, 2026 and geographically references United States. Its severity classification of "medium" signals how the issuing agency weighs the risk of harm if no action is taken - "critical" and "high" tier alerts typically carry direct consumer actions, while "medium" and "low" tend toward informational guidance or monitoring advisories. The category it belongs to - FDA Recalls - determines the consumer-protection framework behind it, which shapes what remedies (refunds, replacements, repairs, or the recall itself) are available to affected consumers and which agency holds statutory responsibility for enforcement.
Most readers skim a notice like this, check whether they are personally affected, and move on. The more useful lens is to verify its scope, source, and timestamp, then compare related notices without assuming that one record proves a broader trend.
Areazine pairs this record with the original agency URL so you can check the primary source before acting. Its related labels are recall, product-safety, fda, Drugs.
What Happened Dabur India Limited initiated a voluntary recall of Med Pride Bacitracin Zinc Ointment due to CGMP deviations, with deficiencies observed during an FDA inspection. The recall is classified as Class II and affects product distributed nationwide in the US.
Which Products Are Affected The affected product is Med Pride, Bacitracin Zinc Ointment, 1oz (28.3g) per tube, 72 tubes per case, Manufactured for: Shield Line LLC, 59 Hook Road, Bayonne, NJ 07002 USA, Made in India, UPC X004WB4LKT. A total of 1185 tubes are involved, from Lot# 022, 023, 024, within expiry. Recall number D-0637-2026.
What You Should Do Consumers should check product lots against the recalled codes and contact the recalling firm for further guidance on returns or refunds.
Why This Matters The recall addresses manufacturing practice deviations in a topical ointment distributed across the United States.
Source FDA recall D-0637-2026, event ID 99137.
Original source: FDA Official Notice ↗
Related FDA Recalls
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Two Areazine-derived peer sets for this FDA recall: nearest notices by body length and by same severity near the same agency date. Peers come from other categories so they are not the same-feed Related list above.
Similar body length
Nearest notices by article body length (964 characters here).
Similar severity timing
Same severity (medium) notices issued closest in time to August 1, 2026.
Frequently Asked Questions
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