Dynarex Wet Wipes Recalled Due to Facility Temperature Exposure
McKesson Medical-Surgical Inc. is recalling three Dynarex wet wipe products that may have been exposed to higher temperatures at the facility before delivery, potentially reducing their effectiveness. All lots received between June and September 2021 are affected.
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: This is an FDA Class III recall with no reported illnesses or injuries. The hazard is theoretical—potential loss of product effectiveness due to temperature exposure—making this a precautionary recall classified as Moderate severity.
Plain-English summary
McKesson Medical-Surgical Inc. is recalling three Dynarex wet wipe products: Nice'n Fresh Baby Wipes (6x6.75 inches), DynaCare Adult Flushable Wipes (9x13 inches), and DynaCare Jr. Flushable Wipes (5x8 inches).
The recall was initiated because facility temperature excursions occurred from June 2021 through August 2021 prior to product delivery. Exposure to these higher temperatures may have impacted the wipes' effectiveness.
The affected products were distributed nationwide. All lots received between June 1, 2021 and September 30, 2021 are included in this recall.
The recalled product
- Product
- a. DYNAREX Nice'n Fresh WIPE, BABY WET 6X6.75" (140/CN12CN/CS) Catalog # 1313. b. DYNAREX DynaCare WIPE, WET FLUSHABLE ADULT 9X13" (24/PK 24PK/CS) Catalog # 1322. c. DYNAREX dynacare WIPE, WET FLUSHABLE JR 5X8" (42/BX 12BX/CS) Catalog # 1324
- Manufacturer
- Mckesson Medical-Surgical Inc. Corporate Office
- Hazard
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)
- unavailable
Distribution
Distributed nationwide across the United States.
Part of a larger recall action
This product is one of 23 recalled by Mckesson Medical-Surgical Inc. Corporate Office under a single FDA (Devices) recall action. The agency files each product separately, so the size of the action is not visible from this page alone.
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