Cardinal Health Recalls ChemoPlus Spill Kits Due to Latex Mismatch
Cardinal Health is recalling ChemoPlus chemotherapy spill kits because the safety goggles inside contain natural rubber latex, despite the kit label stating the product is latex-free.
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, and the hazard involves a labeling error regarding a common allergen (latex) without reported illnesses, fitting the Moderate severity criteria for minor labeling errors or low-risk contamination.
Plain-English summary
Cardinal Health 200, LLC is recalling 11,588 units of ChemoPlus Chemo Spill Kits (Product Code: CT4004). The recall is due to a labeling discrepancy: the kit label states that the product is not made with natural rubber latex, but the safety goggles included within the kits contain natural rubber latex in the goggle strap.
The affected lots are 720708X, 723514X, 728548X, 733515X, 800821X, 802618X, 807122X, 808204X, 811703X, 816569X, 821916X, 826363X, 826065X, 828859X, and 835143X. These kits were distributed nationwide in the United States and internationally to the Bahamas, Canada, Chile, Guam, Israel, and Japan.
The ChemoPlus chemotherapy spill kits are designed for the clean-up and containment of chemotherapy spills. Individuals with a latex allergy should avoid using the safety goggles from these kits. Consumers should check their inventory for the affected product code and lot numbers and contact Cardinal Health for further instructions.
The recalled product
- Product
- ChemoPlus Chemo Spill Kit Product Code:CT4004 Product Usage: ChemoPlus chemotherapy spill kits are for the clean-up and containment of chemotherapy spills
- Manufacturer
- Cardinal Health 200, LLC
- Affected units
- 11,588
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 (15)
- Lot Nubers: 720708X
- 723514X
- 728548X
- 733515X
- 800821X
- 802618X
- 807122X
- 808204X
- 811703X
- 816569X
- 821916X
- 826363X
- 826065X
- 828859X
- 835143X
Distribution
Distributed nationwide across the United States.
Part of a larger recall action
This product is one of 4 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.
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