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.
The agency’s classification
FDA (Devices): Class II
Class II is a situation in which use of or exposure to a violative product may cause temporary or medically reversible adverse health consequences, or where the probability of serious adverse health consequences is remote.
This is the agency’s own classification, taken from its notice. The severity score below is our assessment, not the agency’s. How recall classes work
What this means for you
Our assessment, not the agency’s: severity 2/5 (Moderate).
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.
See all 4 products in this recall →Related recalls
Same manufacturer · Cardinal Health 200, LLC
See all →- SevereCardinal Health Recalls Presource Packs with Medtronic Microstream Components
FDA (Devices) · 2026-10-14
- HighCardinal Health Recalls Gynecological Laparoscopy Kits Due to Handpiece Leakage
FDA (Devices) · 2026-10-07
- HighCardinal Health Recalls Presource Packs Due to Potential Handpiece Leakage
FDA (Devices) · 2026-10-07
- HighCardinal Health Recalls Presource Packs with Leaking Handpieces
FDA (Devices) · 2026-10-07
- HighCardinal Health Recalls Stryker StrykeFlow PS and AHTO Tube Set Kits
FDA (Devices) · 2026-10-07
Same hazard · latex allergen
See all →- ModerateHalyard Laparoscopy Comprehensive Pack II Recalled for Latex Content
FDA (Devices) · 2026-10-14
- ModerateAVID Medical Recalls Halyard Total Joint Kits Due to Latex Labeling Error
FDA (Devices) · 2026-09-02
- ModerateHalyard Total Joint Kits Recalled for Latex Labeling Deficiency
FDA (Devices) · 2026-09-02
- ModerateAVID Medical Recalls Halyard Total Joint Kits for Latex Labeling Deficiency
FDA (Devices) · 2026-09-02
- ModerateAVID Medical Recalls Halyard Total Joint Kits for Latex Labeling Deficiency
FDA (Devices) · 2026-09-02
Similar recalls
- ModerateCardinal Health Recalls ChemoPlus Drug Spill Kits Due to Gown Defects
FDA (Devices) · 2021-02-17
- ModerateCardinal Health Recalls Chemo Spill Kits Due to Gown Defects
FDA (Devices) · 2021-02-17
- ModerateCardinal Health Recalls ChemoPlus Chemo Prep and Admin Kits
FDA (Devices) · 2021-02-17
- ModerateCardinal Health Recalls Protexis Neoprene Surgical Gloves Due to Labeling Error
FDA (Devices) · 2018-12-26
- ModerateCardinal Health Recalls Kendall Spill Kits Due to Gown Defects
FDA (Devices) · 2021-02-17
- ModerateCardinal Health Recalls Protexis Neoprene Surgical Gloves Due to Labeling Errors
FDA (Devices) · 2018-12-26