CLASS II ONGOING Device recall · Reported 22 May 2024 · FDA Enforcement Report
CardinalHealth Curity Flexible Adhesive Bandage X-Large recalled
Cardinal Health 200 is recalling CardinalHealth Curity Flexible Adhesive Bandage X-Large, distributed nationwide in the US. The recall was initiated on 17 Apr 2024 and the FDA has classified it as Class II.
Check your package
Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.
Recall details
- Recall number
- Z-1835-2024
- FDA event ID
- 94407
- Recalling firm
- Cardinal Health 200, Waukegan, IL
- Classification
- Class II
- Status
- Ongoing
- Recall initiated
- 17 Apr 2024
- FDA classified
- 16 May 2024
- Reported
- 22 May 2024
- Type
- Voluntary: Firm initiated
- Customers notified by
- Letter
- Reason category
- Labeling Errors
- Device type
- Other Medical Devices
Timeline
| 17 Apr 2024 | Recall initiated by company | |
| 16 May 2024 | Classified by FDA | +29 days |
| 22 May 2024 | Published in enforcement report | +6 days |
Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.
Reason for recall
Potential contamination of the product with latex adhesive residual.
Product as listed by the FDA
CardinalHealth Curity Flexible Adhesive Bandage X-Large 2 x 3.75 in. (5.1 x 9.5 cm), Model 44102, Sterile, Hypoallergenic.
Where it was distributed
US Nationwide distribution.
Questions about this recall
Why was it recalled?
Potential contamination of the product with latex adhesive residual.
Which lots are affected?
Lot #A14722, UDI-DI: 50192253049907 (CS), 20192253049906 (BX)
Where was it sold?
US Nationwide distribution.
What should I do if I have it?
Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.
What does Class II mean?
Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.
Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.
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