The Recall Desk
ModerateFDA (Drugs)·D-1327-2022·Announced 2022-08-17

Antiseptic Alcohol Swabs Recalled Due to Improper Storage Conditions

McKesson is recalling Dynarex Alcohol Swabsticks nationwide because products were stored outside the conditions specified on the drug label.

What this means for you

Minor labeling or packaging issue, or a voluntary precautionary recall. Risk of harm is low but real — follow the manufacturer's instructions.

Our severity reasoning: FDA Class II recall with no reported illnesses or injuries. The hazard is a manufacturing compliance deviation (improper storage) without documented evidence of product harm, classifying this as a precautionary recall.

Plain-English summary

McKesson Medical-Surgical Inc. is recalling Dynarex Alcohol Swabsticks, an over-the-counter antiseptic product. The swabs are packaged as 50 4-inch saturated individual packets per box.

The recall was initiated due to Good Manufacturing Practice (CGMP) deviations: products were stored outside the conditions specified on the drug label. The affected product includes NDC 67777-300-01 (current) and NDC 67777-120-10 (discontinued), with Part# 1203. Distribution was nationwide in the United States.

The recalled product

Product
ALCOHOL (ALCOHOL)
Brand
ALCOHOL
Manufacturer
Mckesson Medical-Surgical Inc. Corporate Office
Category
Drug — Topical Antiseptic
Hazard
  • improper-storage

Is your product affected?

Check your packaging against the codes below. If any of them match, the product is part of this recall.

Lot numbers (1)

  • Part# 1203

UPCs (2)

  • 0616784120324
  • 0616784120423

Distribution

Distributed nationwide across the United States.

Related recalls

Same category