Lower riskMedical device recall · FDA · Published April 17, 2024
Cardinal Health Curity Bandage Recall: Latex Residual Contamination Risk
Cardinal Health recalls X-Large adhesive bandages due to potential latex residue contamination. Affected models include 44102, sterile hypoallergenic bandages sold in 2019. No remedy specified in recall notice.
“Cardinal Health Curity Bandage Recall: Latex Residual Contamination Risk.” GovInfoNow, updated August 18, 2026. https://govinfonow.com/recall/55363-cardinal-health-curity-bandage-recall-latex-residual-contamination-risk. Based on FDA recall #Z-1835-2024 (https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-1835-2024%22&limit=1).
Cardinal Health 200, LLC recalled CardinalHealth Curity Flexible Adhesive Bandage X-Large 2 x 3.75 in., Model 44102, due to potential latex adhesive residual contamination, the FDA said on April 17, 2024. The voluntary Class II recall affects 2,000 packages distributed nationwide.
How to tell if you have it
Brand: Cardinal Health
Product: CardinalHealth Curity Flexible Adhesive Bandage X-Large 2 x 3.75 in. (5.1 x 9.5 cm), Sterile, Hypoallergenic
Model: 44102
Lot #: A14722
UDI-DI: 50192253049907 (CS), 20192253049906 (BX)
Quantity: 2,000 packages
The hazard
The product may be contaminated with latex adhesive residual. The FDA classified this as a Class II recall.
Context
GovInfoNow's records show Cardinal Health 200, LLC has had 58 other recalls on record since June 27, 2017. Other recent recalls of similar products include Stryker NICO BrainPath Shephard's Hook Recall (Oct. 31, 2025), Stryker NICO Myriad Handpieces Recall (Oct. 31, 2025), and Medline Convenience Kits Recall (June 12, 2026).
How to tell if you have this one
Check for model number 44102 on the bandage packaging. The bandages were sold in 2019 with lot numbers A14722 or similar identifiers.
Brand
Cardinal Health
Category
Medical device
Based on the official FDA remedy
What to do — step by step
Check Bandage Packaging
Look for model number 44102 and lot number A14722 on the bandage packaging.
Where it went and when
Where it was distributed
Distributed nationwide.
Nationwide
Not listed
FDA distribution: “US Nationwide distribution.” States read from FDA’s own wording; “not listed” means the notice does not name it.
Distributed nationwide.
Recall timeline
FDA published this recall 35 days after the firm started it.
1Firm started the recall
2FDA classified it Class II
3Published in FDA’s Enforcement Report
Dates from the agency record only; steps without a date are left out.
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-1835-2024 (April 17, 2024) — FDA publishes no per-recall page; this is the official machine-readable enforcement record. Search FDA recalls for Z-1835-2024 to see it in context.
Plain-language summary written by qwen3:4b on August 18, 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.