Cook, Inc. Recalls Various Medical Device Sets Due to Incorrect Expiration Dates
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Cook, Incorporated is recalling several medical device sets, including Blue Rhino and Central Venous Catheter sets, because labels display incorrect, extended expiration dates.
What this Health Canada recall tells you, and what most readers miss
This notice was issued by Health Canada on April 3, 2026 and geographically references Canada. Its severity classification of "medium" signals how the issuing agency weighs the risk of harm if no action is taken — "critical" and "high" tier alerts typically carry direct consumer actions, while "medium" and "low" tend toward informational guidance or monitoring advisories. The category it belongs to — Product & Food Recalls — determines the regulatory framework behind it, which shapes what remedies (refunds, replacements, recalls, evacuations) are available to affected individuals and who holds statutory responsibility for enforcement.
Most readers skim a notice like this, check whether they are personally affected, and move on. The more useful lens is to read it as a data point about the issuing system: how quickly Health Canada detected the hazard, how precise the geographic or product-identifier scope is, and whether similar notices have clustered in the same category or region in the last 90 days. Cluster patterns frequently precede a broader regulatory action — a single localized Health Canada recall is isolated; three of them within a quarter often indicate a supply-chain, infrastructure, or seasonal driver that will keep producing notices until something structural changes.
For decision-making, Areazine pairs each alert with the original agency URL, the full agency name, and a timestamp so you can verify the notice against the primary source before acting on it. Tags on this item (recall, product-safety, health-canada, medical-device) map to related alerts in the same area of risk — browsing them together gives a clearer picture than any single notice alone, because the shape of an ongoing issue only becomes visible across multiple sequential alerts.
What Happened
Cook, Incorporated has issued a recall for several medical device sets because the product labels display incorrect expiration dates. An internal investigation determined that errors occurred during the process of setting expiration dates based on the earliest expiring component. This resulted in some products being labeled with shelf-lives that are longer than their actual validated duration.
Which Products Are Affected
The recall involves several device types and specific lot numbers, including the Approach® CTO Micro Wire Guide and Wayne Pneumothorax Set. Specific lot and model details provided include:
Blue Rhino® G2-Multi Percutaneous Tracheostomy Introducer Set
- Lot 15151627 (Model C-PTIS-100-UNL-HC-G-EU)
- Lot 16189597 (Model C-PTIS-100-HC-G-EU)
- Lot 16175956 (Model C-PTIS-100-HC-G-EU)
- Lot 16175949 (Model C-PTIS-100-UNS-HC-G-EU)
Cook Five Lumen Central Venous Catheter Set
- Lot 15478180 (Model C-UQLM-1001J-ABRM-HC-RD)
Triple Lumen Central Venous Catheter Set W/Spectrum Glide Antimicrobial
- Lot 16532975 (Model C-UTLM-701J-ABRM-HC-RD-CAH)
- Lot NS15660282 (Model C-UTLM-501J-ABRM-HC-CAH)
- Lot 15687199 (Model C-UTLM-701J-RSC-ABRM-HC-RD-CAH)
- Lot NS15597521 (Model C-UTLM-501J-PED-ABRM-HC)
What You Should Do
Healthcare facilities and consumers should immediately check their inventory for the affected lot and model numbers. If affected products are found, they should not be used. For more information, contact Cook, Incorporated at 750 Daniels Way, Bloomington, Indiana, 47404.
Why This Matters
Using medical devices beyond their intended shelf-life can lead to component degradation or loss of sterility, which may pose risks to patient health.
Source
This recall is based on information provided by Health Canada.
Original source: Health Canada Official Notice ↗
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