Cardinal Health Recalls In-View Clear Leggings Due to Manufacturing Variance
Cardinal Health is recalling In-View Clear Leggings Sterile because a manufacturing variance causes the plastic film to stick, potentially 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. The hazard is a functional defect (sticking) that prevents proper application, but the source text does not report any injuries, illnesses, or deaths, fitting the criteria for a moderate severity recall.
Plain-English summary
Cardinal Health 200, LLC is recalling 28,417 units of In-View Clear Leggings Sterile. The recall was initiated because a manufacturing variance in the plastic film used to manufacture the products is causing the drapes and leggings to stick.
This defect may prevent the products from being unfolded and applied properly. The affected products were distributed nationwide to numerous U.S. states and territories, as well as to Australia and Canada. Specific lot numbers and expiration dates are listed in the official recall documentation.
Healthcare facilities and consumers should stop using the affected products and contact Cardinal Health for further instructions or a return.
The recalled product
- Product
- In-View Clear Leggings Sterile
- Manufacturer
- Cardinal Health 200, LLC
- Affected units
- 28,417
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 (9)
- Catalog Number 8430
- Lot number's: 20JKS003 (expiration date:2025-09-01)
- 20JKS004 (expiration date:2025-09-01)
- 20JKS005 (expiration date:2025-09-01)
- 20KKS047 (expiration date:2025-10-01)
- 20KKS050 (expiration date:2025-10-01)
- 20LKS63 (expiration date:2025-11-01)
- 20LKS075 (expiration date:2025-11-01)
- and 20MKS003 (expiration date:2025-12-01).
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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