RegWardenFDA facility compliance records
Recall

Class III — Canadian Hospital Specialties

Recalling firmCanadian Hospital Specialties Ltd.
Registered facilityCANADIAN HOSPITAL SPECIALTIES LTD (the firm's only registered facility)
ClassificationClass III
StatusTerminated
ReasonSome of the labels of the kits for product code 10-4001 in the specified lots have an illegible barcode which prevents successful scanning of the package.
ProductMED-RX UROLOGICAL CYSTO/BLADDER IRRIGATION SET, REF 10-4001
Quantity9100 units
DistributionUS
Initiated2022-08-19
Classified2022-11-11
Terminated2023-03-20
Recall numberZ-0202-2023
InitiationVoluntary: Firm initiated

Source: U.S. FDA via openFDA (opens in a new tab) (device registration & enforcement). Data as of 2026-10-06. Verify this recall record at FDA → (opens in a new tab)

Cite this record

RegWarden. “Class III recall — Canadian Hospital Specialties (Z-0202-2023).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/90926/

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