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Lower risk Medical device recall · FDA · Published February 25, 2021

Cardinal Health In-View Clear Leggings Sterile Recall: Sticking Drapes May Prevent Proper

Cardinal Health recalls sterile In-View Clear Leggings due to plastic film manufacturing issues causing drapes to stick, potentially preventing proper application. Affected lots expire through December 2025.

Plain-English summary generated from official FDA data by GovInfoNow · Published by Carlos Caban · How we make summaries

🇺🇸 FDA recall #Z-1300-2021Medical deviceCardinal Health ›
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Contact the company

Recalling firmCardinal Health 200, LLC3651 Birchwood Dr · Waukegan, IL 60085-8337
✎ GovInfoNow plain-language explainer

Cardinal Health is recalling sterile In-View Clear Leggings because a manufacturing issue causes the drapes to stick, which might make them difficult to unfold and apply correctly. This could lead to improper use of the medical products. Read more at govinfonow.com/recall/63223-cardinal-health-in-view-clear-leggings-sterile-recall-sticking-drapes.

Source Summary by GovInfoNow · govinfonow.com/recall/63223-cardinal-health-in-view-clear-leggings-sterile-recall-sticking-drapes · Updated August 19, 2026 · FDA enforcement record: FDA #Z-1300-2021

Cite this page

“Cardinal Health In-View Clear Leggings Sterile Recall: Sticking Drapes May Prevent Proper.” GovInfoNow, updated August 19, 2026. https://govinfonow.com/recall/63223-cardinal-health-in-view-clear-leggings-sterile-recall-sticking-drapes. Based on FDA recall #Z-1300-2021 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1300-2021%22&limit=1).

The FDA announced on Feb. 25, 2021, that Cardinal Health 200, LLC is recalling In-View Clear Leggings Sterile due to a manufacturing variance causing the products to stick. This may prevent proper unfolding and application. The recall involves 28,417 units distributed nationwide and to Australia and Canada.

How to tell if you have it

  • Brand: Cardinal Health
  • Product: In-View Clear Leggings Sterile
  • Catalog Number: 8430
  • Lot numbers: 20JKS003, 20JKS004, 20JKS005, 20KKS047, 20KKS050, 20LKS63, 20LKS075, 20MKS003
  • Expiration dates: 2025-09-01, 2025-10-01, 2025-11-01, 2025-12-01

The hazard

A manufacturing variance in the plastic film causes the drapes and leggings to stick. This may prevent the products from being unfolded and applied properly.

Context

GovInfoNow's records show Cardinal Health 200, LLC has 59 other recalls on record since 2017-06-27. Other recent recalls of similar products include Presource Packs with Microstream Components Risk of Delayed Treatment (2026-08-19), Cardinal Health 200, LLC recalls Presource Packs Containing Stryker StrykeFlow PS and AHTO tube sets (2026-08-18), and Cardinal Health 200, LLC recalls Presource Convenience Kits (2026-08-10). Other recent recalls of similar products include Medline Surgical Drapes Recall: Sterility Risk from Calibration Issues (2026-01-07), Medline Convenience Kits Recall: Risk of Sterile Packaging Breach (2026-06-12), and Medline Convenience Kits Recall: Potential Sterility Breach in Packaging (2026-06-12).

How to tell if you have this one

Check for lot numbers: 20JKS003-005 (expiring September 2025) or 20KKS047-050 (expiring October 2025) or 20LKS63-075 (expiring November 2025) or 20MKS003 (expiring December 2025).

  • Brand
    Cardinal Health
  • Category
    Medical device
FDA recall event · 5 products

All 5 products in this recall

FDA lists each product line separately under one recall event. Check your product description, lot or code numbers against each row. Every row shares the hazard and remedy on this page.

  • Classification
    Class II
  • Status
    Terminated
  • Distribution
    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.
Recall numberProduct, codes & lotsQuantity
Z-1300-2021In-View Clear Leggings Sterile; 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).28417 units
Z-1301-2021In-View Clear Leggings Sterile Non-Sterile; Catalog Number 8430N; Lot number's: 3290DR1 and 3300DR11020 units
Z-1302-2021In-View Clear Leggings Bulk Non-Sterile; 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, 3440DR121343 units
Z-1303-2021Femoral Angiography Drape Sterile; Catalog Number 29560; Lot number's: 20LQR067 (expiration date: 2025-11-01) and 20MQR023 (expiration date: 2025-12-01)936 units
Z-1304-2021Femoral Angiography Drape Bulk Non-Sterile; Catalog Number 29560NC; Lot number's: 2450ER1, 2660ER1, 2960ER1, 2450ER2, 2660ER2, 2960ER2, 2460ER1, 2670ER1, 2970ER1, 2460ER2, 2670ER2, 2970ER2, 2470ER1, 2690ER1, 3030ER1, 2470ER2, 2690ER2, 3030ER2, 2480ER1, 2720ER1, 3040ER1, 2480ER2, 2720ER2, 3040ER2, 2510ER1, 2730ER1, 3080ER2, 2510ER2, 2730ER2, 3090ER1, 2520ER1, 2740ER1, 3090ER2, 2520ER2, 2740ER2, 3100ER1, 2530ER1, 2750ER1, 3100ER2, 2530ER2, 2750ER2, 3150ER1, 2540ER1, 2760ER1, 3160ER1, 2600ER2, 2760ER2, 3170ER1, 2610ER1, 2820ER1, 3180ER1, 2610ER2, 2820ER2, 3210ER1, 2620ER1, 2830ER1, 3290FR1, 2620ER2, 2830ER2, 3490FR1, 2650ER1, 2860ER1, 2650ER2, 2950ER283213 units
Based on the official FDA remedy

What to do — step by step

  1. Check Product Lot Number

    Look for lot numbers on the packaging: 20JKS003-005 (expiring September 2025), 20KKS047-050 (expiring October 2025), 20LKS63-075 (expiring November 2025), or 20MKS003 (expiring December 2025).

Where it went and when

Where it was distributed

Distributed nationwide and abroad; the notice names 44 states.

Alaska: named in the noticeAKMaine: nationwideMEVermont: nationwideVTNew Hampshire: named in the noticeNHWashington: named in the noticeWAIdaho: named in the noticeIDMontana: nationwideMTNorth Dakota: named in the noticeNDMinnesota: named in the noticeMNIllinois: named in the noticeILWisconsin: named in the noticeWIMichigan: named in the noticeMINew York: named in the noticeNYRhode Island: nationwideRIMassachusetts: named in the noticeMAOregon: named in the noticeORNevada: named in the noticeNVWyoming: nationwideWYSouth Dakota: named in the noticeSDIowa: named in the noticeIAIndiana: named in the noticeINOhio: named in the noticeOHPennsylvania: named in the noticePANew Jersey: named in the noticeNJConnecticut: named in the noticeCTCalifornia: named in the noticeCAUtah: named in the noticeUTColorado: named in the noticeCONebraska: named in the noticeNEMissouri: named in the noticeMOKentucky: named in the noticeKYWest Virginia: named in the noticeWVVirginia: named in the noticeVAMaryland: named in the noticeMDDelaware: named in the noticeDEArizona: named in the noticeAZNew Mexico: named in the noticeNMKansas: nationwideKSArkansas: named in the noticeARTennessee: named in the noticeTNNorth Carolina: named in the noticeNCSouth Carolina: named in the noticeSCDistrict of Columbia: named in the noticeDCOklahoma: named in the noticeOKLouisiana: named in the noticeLAMississippi: named in the noticeMSAlabama: named in the noticeALGeorgia: named in the noticeGAHawaii: named in the noticeHITexas: named in the noticeTXFlorida: named in the noticeFL

FDA distribution: “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…” States read from FDA’s own wording; “not listed” means the notice does not name it.

Named in the notice: Alabama, Alaska, Arizona, Arkansas, California, Colorado, Connecticut, Delaware, District of Columbia, Florida, Georgia, Hawaii, Idaho, Illinois, Indiana, Iowa, Kentucky, Louisiana, Maryland, Massachusetts, Michigan, Minnesota, Mississippi, Missouri, Nebraska, Nevada, New Hampshire, New Jersey, New Mexico, New York, North Carolina, North Dakota, Ohio, Oklahoma, Oregon, Pennsylvania, South Carolina, South Dakota, Tennessee, Texas, Utah, Virginia, Washington, West Virginia, Wisconsin.

Recall timeline

FDA terminated this recall 2.9 years after the firm started it.

1. Firm started the recall: Feb 25, 202112. FDA classified it Class II: Mar 24, 202123. Published in FDA’s Enforcement Report: Mar 31, 202134. FDA terminated the recall: Jan 9, 2024420212024
  1. Firm started the recall
  2. FDA classified it Class II
  3. Published in FDA’s Enforcement Report
  4. FDA terminated the recall

Dates from the agency record only; steps without a date are left out.

✎ GovInfoNow

Questions people ask

From the GovInfoNow team · based on the FDA notice · How we make summaries

Are there any safety risks from using this product?

The product may stick together and prevent proper application, but this does not pose a risk of injury or serious harm in normal use.

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Keep exploring

Where this comes from

The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.

  • Official source: FDA Recall #Z-1300-2021 (February 25, 2021) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-1300-2021 to see it in context.
  • Plain-language summary written by qwen3:4b on August 19, 2026, from the official record above. Not reviewed by a person — if it conflicts with the FDA notice, the notice is correct. Report an error on this page.
  • GovInfoNow is an independent service and is not a government agency. We republish official FDA recall data; we don’t issue, amend or administer recalls.
GovInfoNow is an independent guide. We are not FDA or any government agency. Always confirm details with the official recall.Data: CPSC · FDA · NHTSA · USDA