Cardinal Health Recalls ChemoPlus Goggles Due to Latex Mislabeling
Cardinal Health is recalling ChemoPlus Protective Wrap-around Goggles because the kit labels state they are latex-free, but the goggle straps contain natural rubber latex.
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 3/5 (High).
Real risk of harm even if no illness or injury has been reported yet. Stop using the product and follow the agency's guidance.
Our severity reasoning: The recall involves allergen mislabeling on a common allergen (natural rubber latex), which corresponds to a High severity score per the rubric.
Plain-English summary
Cardinal Health 200, LLC is recalling 3,236 units of ChemoPlus Protective Wrap-around Goggles (Product Code: DP5030G). These goggles are part of ChemoPlus chemotherapy spill kits used for the clean-up and containment of chemotherapy spills.
The recall was initiated because the kit labels state that the product is not made with natural rubber latex. However, the safety goggles within the kits contain natural rubber latex in the goggle strap. This discrepancy poses a risk to individuals with latex allergies.
The affected units were distributed worldwide, including in the US and foreign locations such as the Bahamas, Canada, Chile, Guam, Israel, and Japan. Individuals with latex allergies should stop using the affected goggles and contact Cardinal Health for a replacement or refund.
The recalled product
- Product
- ChemoPlus Protective Wrap-around Goggles Product Code:DP5030G Product Usage: ChemoPlus chemotherapy spill kits are for the clean-up and containment of chemotherapy spills
- Manufacturer
- Cardinal Health 200, LLC
- Affected units
- 3,236
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: 235508X
- 303205X
- 305701X
- 307708X
- 308126X
- 309206X
- 319602X
- 320504X
- 323204X
- 410837X
- 413643X
- 414326X
- 416430X
- 422701X
- 430016X
- 430442X
- 431828X
- 434226X
- 434528X
- 506449X
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
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