Data Foundry

Medical device recalls 2019

ChemoPlus Chemo Spill Kit — Class II medical device recall Z-1286-2019

Terminated recall by Cardinal Health 200, LLC, reported 2019-05-15, distributed nationwide. Kit label states not made with natural rubber latex,however safety goggles within the kits contain natural rub

Recall numberZ-1286-2019
Product typeMedical device
ClassificationClass II
StatusTerminated
Voluntary or mandatedVoluntary
Recalling firmCardinal Health 200, LLC, Mansfield, MA, United States
Recall initiated2019-03-22
Classified2019-05-06
Reported by FDA2019-05-15
Terminated2021-08-06
DistributedNationwide (US)
Countries outside the USBS, CA, CL, IL, JP
Quantity5,415
Reason classeslabeling
Lot numbers235609, 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 and 16 more

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

Reason for recall

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

Machine access

This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/Z-1286-2019. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.

Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.