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Recall data is sourced from official U.S. government agencies (CPSC, FDA, NHTSA, USDA) and processed using AI to improve readability. This site is not affiliated with or endorsed by any government agency. Always refer to the original agency notice for authoritative information.

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Medium RiskFDA Device

Cardinal Health 200, LLC: Kit label states not made with natural rubber latex,however safety goggles within the kits contain natural rubber latex in the goggle strap

Agency Publication Date: May 6, 2019
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Affected Products

Product: ChemoPlus Chemo Spill Kit Product Code:CT4004 Product Usage: ChemoPlus chemotherapy spill kits are for the clean-up and containment of chemotherapy spills

Lot Nubers: 720708X, 723514X, 728548X, 733515X, 800821X, 802618X, 807122X, 808204X, 811703X, 816569X, 821916X, 826363X, 826065X, 828859X, 835143X

Lot Numbers:
Nubers
Product: ChemoPlus Chemo Spill Kit Product Code:DP5016K Product Usage: ChemoPlus chemotherapy spill kits are for the clean-up and containment of chemotherapy spills

Lot Numbers: 708265X, 709766X, 712108X, 713853X, 719505X, 723645X, 726111X, 727029X, 730304X, 735321X, 803307X, 803990X, 808097X, 809318X, 812914X, 815537X, 821910X, 825016X, 826407X, 833752X

Lot Numbers:
Numbers
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

Lot Numbers: 235508X, 303205X, 305701X, 307708X, 308126X, 309206X, 319602X, 320504X, 323204X, 410837X, 413643X, 414326X, 416430X, 422701X, 430016X, 430442X, 431828X, 434226X, 434528X, 506449X, 619595X, 622266X, 624614X, 625363X, 629806X, 703411X, 705165X, 706224X, 708004X, 710351X, 712123X, 719186X, 720507X, 723650X, 729905X, 734723X, 803018X, 812171X, 817809X, 823430X, 825704X, 826721X

Lot Numbers:
Numbers
Product: ChemoPlus Chemo Spill Kit, Home Health Kit Product Code:DP5108K Product Usage: ChemoPlus chemotherapy spill kits are for the clean-up and containment of chemotherapy spills

Lot Numbers: 235609, 303919X, 308148X, 311604X, 312606X, 318318X, 324933X, 328469X, 332206X, 333619X, 400228X, 404307X, 407209X, 410401X, 411560X, 413642X, 421208X, 425562X, 431002X, 433930X, 500815X, 502094X, 508526X, 509804X, 518003X, 523602X, 526504X, 531034X, 535770X, 604188X, 608358X, 611322X, 613451X, 621800X, 625601X, 628817X, 631332X, 634400X, 704641X, 707612X, 711572X, 714407X, 717902X, 723502X, 727719X, 731410X, 735208X, 802308X, 812169X, 815024X, 814519X, 817810X, 827112X, 827610X, 830967X, 833057X

Lot Numbers:
Numbers

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 82535
Status: Resolved
Manufacturer: Cardinal Health 200, LLC
Manufactured In: United States
Units Affected: 4 products (11588; 21082; 3236; 5415)

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AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.

Sources: FDA iRES · Raw API Response

openFDA Disclaimer: This recall information is sourced from the openFDA API. Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Refer to the openFDA terms of service for more information.