The Recall Desk
ModerateFDA (Devices)·Z-1302-2021·Announced 2021-03-31

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.

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: 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
Category
Medical Device — Surgical Drapes and Leggings
Hazard
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

Distributed nationwide across the United States.

The notice also names 45 states specifically:

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.

See all 5 products in this recall →

Related recalls

Same manufacturer · Cardinal Health 200, LLC

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Same hazard · functional defect

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