Z-1302-2021 Class II Terminated

Recalled by Cardinal Health 200, LLC — Waukegan, IL

FDA device recall Z-1302-2021 was initiated by Cardinal Health 200, LLC on February 25, 2021 and is designated Class II. Reason for recall: Cardinal Health has determined that a manufacturing variance in a plastic film used to manufacture these products is causing the drapes and leggings to stick , which may prevent the products from bein… The recall status is terminated (terminated January 9, 2024). Affected quantity: 21343 units.

Recall Details

Product Type
Devices
Report Date
March 31, 2021
Initiation Date
February 25, 2021
Termination Date
January 9, 2024
Voluntary/Mandated
Voluntary: Firm initiated
Product Quantity
21343 units

Product Description

In-View Clear Leggings Bulk Non-Sterile

Reason for Recall

Cardinal Health has determined that a manufacturing variance in a plastic film used to manufacture these products is causing the drapes and leggings to stick , which may prevent the products from being unfolded and applied properly.

Distribution Pattern

Distributed nationwide to AK, AL, AR, AZ, CA, CO, CT, DC, DE, FL, GA, HI, IA, ID, IL, IN, KY, LA, MA, MD, MI, MN, MO, MS, NC, ND, NE, NH, NJ, NM, NV, NY, OH, OK, OR, PA, SC, SD, TN, TX, UT, VA, WA, WI, WV. Distributed also to Australia and Canada.

Code Information

Catalog Number 8430NA; Lot number's: 2460DR2, 2550DR1, 2660DR1, 2470DR2, 2580DR1, 2690DR1, 2480DR2, 2580DR2, 2720DR1, 2520DR1, 2600DR1, 2730DR1, 2530DR1, 2600DR1, 3290DR1, 2540DR1, 2610DR1 3310DR1, 2540DR2, 2650DR1, 3440DR1