The Recall Desk
HighFDA (Devices)·Z-1285-2019·Announced 2019-05-15

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.

What this means for you

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
Category
Medical Device — Personal Protective Equipment
Hazard
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

Same manufacturer · Cardinal Health 200, LLC

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Same hazard · latex allergy

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