Cardinal Health Recalls In-View Clear Leggings Due to Manufacturing Variance
Cardinal Health is recalling In-View Clear Leggings because a manufacturing variance causes the product to stick, preventing proper application.
The agency’s classification
FDA (Devices): Class II
Class II is a situation in which use of or exposure to a violative product may cause temporary or medically reversible adverse health consequences, or where the probability of serious adverse health consequences is remote.
This is the agency’s own classification, taken from its notice. The severity score below is our assessment, not the agency’s. How recall classes work
What this means for you
Our assessment, not the agency’s: severity 2/5 (Moderate).
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: The recall is classified as FDA Class II, but the source text describes a functional defect (sticking) that prevents proper application without reporting any injuries, illnesses, or hospitalizations. This aligns with the rubric for moderate severity involving low-risk issues or voluntary precautionary measures where harm is not yet reported.
Plain-English summary
Cardinal Health 200, LLC is recalling 1,020 units of In-View Clear Leggings, both sterile and non-sterile versions. The affected products are identified by Catalog Number 8430N and Lot numbers 3290DR1 and 3300DR1.
The recall was initiated because a manufacturing variance in the plastic film used to manufacture these products is causing the drapes and leggings to stick. This defect may prevent the products from being unfolded and applied properly.
The products were distributed nationwide to 44 states and the District of Columbia, as well as to Australia and Canada. The source text does not specify instructions for consumers or healthcare providers on how to handle the recalled items.
The recalled product
- Product
- In-View Clear Leggings Sterile Non-Sterile
- Manufacturer
- Cardinal Health 200, LLC
- Affected units
- 1,020
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 (2)
- Catalog Number 8430N
- Lot number's: 3290DR1 and 3300DR1
Distribution
Part of a larger recall action
This product is one of 5 recalled by Cardinal Health 200, LLC 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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