Cardinal Health Recalls In-View Clear Leggings Due to Sticking Defect
Cardinal Health is recalling In-View Clear Leggings because a manufacturing variance causes the plastic film 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, fitting the criteria for a moderate severity precautionary recall.
Plain-English summary
Cardinal Health 200, LLC is recalling In-View Clear Leggings Bulk Non-Sterile. The recall involves 21,343 units of the product, which was distributed nationwide to numerous US states as well as Australia and Canada.
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.
Healthcare facilities and consumers who have these products should stop using them and contact Cardinal Health for instructions on how to return the items or obtain a replacement.
The recalled product
- Product
- In-View Clear Leggings Bulk Non-Sterile
- Manufacturer
- Cardinal Health 200, LLC
- Affected units
- 21,343
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 (20)
- Catalog Number 8430NA
- Lot number's: 2460DR2
- 2550DR1
- 2660DR1
- 2470DR2
- 2580DR1
- 2690DR1
- 2480DR2
- 2580DR2
- 2720DR1
- 2520DR1
- 2600DR1
- 2730DR1
- 2530DR1
- 3290DR1
- 2540DR1
- 2610DR1 3310DR1
- 2540DR2
- 2650DR1
- 3440DR1
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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