RegWardenFDA facility compliance records
Recall

Class II — Canadian Hospital Specialties Ltd.

Recalling firmCanadian Hospital Specialties Ltd.
Registered facilityCANADIAN HOSPITAL SPECIALTIES LTD (the firm's only registered facility)
ClassificationClass II
StatusOngoing
ReasonA customer found product with incomplete seals of P/N 20400161S, lot #185198 which can lead to non-sterile product and patient safety concerns. CHS has validated this complaint.
ProductProduct Name: HIGH FLOW INSUFFLATION TUBING (with Filter) Model/Catalog Number: 20400161S Product Description: Laparoscopic Insufflator
Quantity6300 units
DistributionUS Nationwide distribution in the state of MA.
Initiated2024-06-11
Classified2024-07-17
Recall numberZ-2408-2024
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 II recall — Canadian Hospital Specialties Ltd. (Z-2408-2024).” Compiled from U.S. FDA public records (openFDA; FDA Data Dashboard). Data as of 2026-10-06. https://regwarden.com/recall/94834/

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