Canadian Hospital Specialties

Complete recall history across all FDA and CPSC categories — 4 total recalls

Canadian Hospital Specialties appears in recall records across 1 category. This page consolidates all FDA food, drug, and medical device enforcement actions, plus CPSC consumer product recalls associated with this company. Recall data is sourced from openFDA and CPSC public databases.

Device Recalls (4)

FDA medical device enforcement actions by Canadian Hospital Specialties

Date Product Reason Class
Aug 19, 2022 MED-RX UROLOGICAL CYSTO/BLADDER IRRIGATION SET, REF 10-4001 Some of the labels of the kits for product code 10-4001 in the specified lots... Class III
Jul 16, 2019 MED-RX POLYURETHANE FEEDING TUBES: a) 5Fr X 16" (40cm), REF 54-1650R b) 6.... The firm received a complaint that the connector detached from the feeding tube. Class II
Dec 1, 2018 MED-RX POLYURETHANE FEEDING TUBE For Pediatric Use with Orange Radioplaque St... The product may be packaged with a 5FR X 24 length Feeding tube instead of a... Class II
Jun 11, 2018 MED-RX, Ref 54-1650R 5Fr X 16 inch (40cm) Polyurethane Feeding Tube For Pedia... The product may be packaged with the incorrect length of feeding tube as labe... Class II

Frequently Asked Questions

A high number of recalls does not necessarily indicate that a company is unsafe. Large manufacturers that produce thousands of products across multiple categories will statistically appear in recall databases more frequently. What matters more is the severity of each recall (Class I being the most serious), the speed of response, and whether the company proactively identified and addressed the issue. Companies with robust safety programs often catch problems earlier.

Food, drug, and medical device recall data comes from the FDA's openFDA enforcement database, which contains all FDA enforcement reports. Consumer product recall data comes from the U.S. Consumer Product Safety Commission (CPSC). Both sources are public government databases that are updated regularly. RecallCheck aggregates these sources to provide a unified view of a company's recall history.

The FDA classifies recalls into three categories. Class I is the most serious — there is a reasonable probability that use of or exposure to the product will cause serious adverse health consequences or death. Class II means the product may cause temporary or medically reversible health problems, or the probability of serious consequences is remote. Class III is the least serious — the product is unlikely to cause adverse health consequences. CPSC product recalls do not use this classification system.

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