Cardinal Health Recalls ChemoPlus Spill Kits Due to Latex Inconsistency
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: This is an FDA Class II recall involving a labeling error regarding a common allergen (latex). The rubric classifies minor labeling errors and low-risk contamination as Moderate (Score 2), as no injuries or illnesses are reported in the source text.
Plain-English summary
Cardinal Health 200, LLC is recalling 21,082 units of ChemoPlus Chemo Spill Kits (Product Code: DP5016K). The recall was initiated because the kit label states 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 lot numbers are 708265X, 709766X, 712108X, 713853X, 719505X, 723645X, 726111X, 727029X, 730304X, 735321X, 803307X, 803990X, 808097X, 809318X, 812914X, 815537X, 821910X, 825016X, 826407X, and 833752X. 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 lot numbers against the list provided and contact Cardinal Health for further instructions or a replacement.
The recalled product
- Product
- ChemoPlus Chemo Spill Kit Product Code:DP5016K Product Usage: ChemoPlus chemotherapy spill kits are for the clean-up and containment of chemotherapy spills
- Manufacturer
- Cardinal Health 200, LLC
- Affected units
- 21,082
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 (20)
- Lot Numbers: 708265X
- 709766X
- 712108X
- 713853X
- 719505X
- 723645X
- 726111X
- 727029X
- 730304X
- 735321X
- 803307X
- 803990X
- 808097X
- 809318X
- 812914X
- 815537X
- 821910X
- 825016X
- 826407X
- 833752X
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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