CLASS II ONGOING Device recall · Reported 15 Apr 2026 · FDA Enforcement Report

Medical Thal-Quick Chest Tube Tray: Reference recalled

Cook is recalling Medical Thal-Quick Chest Tube Tray: Reference. The recall was initiated on 5 Mar 2026 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesReference Part Number C-TQTSY-3200, UDI (01)00827002072428(17)270221(10)NS15796862X, Lot Number NS15796862X; Reference Part Number C-TQTSY-3200, UDI (01)00827002072428(17)270301(10)NS15881832X, Lot Number NS15881832X.
Quantity recalled2 units

Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.

Recall details

Recall number
Z-1790-2026
FDA event ID
98495
Recalling firm
Cook, Bloomington, IN
Classification
Class II
Status
Ongoing
Recall initiated
5 Mar 2026
FDA classified
6 Apr 2026
Reported
15 Apr 2026
Type
Voluntary: Firm initiated
Customers notified by
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
Reason category
Other Reasons

Timeline

5 Mar 2026Recall initiated by company
6 Apr 2026Classified by FDA+32 days
15 Apr 2026Published in enforcement report+9 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

Products from the affected device lots were labeled with expiration dates that exceed the true shelf life.

Product as listed by the FDA

COOK MEDICAL Thal-Quick Chest Tube Tray: Reference Part Number C-TQTSY-3200, Order Number G07242

Where it was distributed

Worldwide distribution.

Questions about this recall

Why was it recalled?

Products from the affected device lots were labeled with expiration dates that exceed the true shelf life.

Which lots are affected?

Reference Part Number C-TQTSY-3200, UDI (01)00827002072428(17)270221(10)NS15796862X, Lot Number NS15796862X; Reference Part Number C-TQTSY-3200, UDI (01)00827002072428(17)270301(10)NS15881832X, Lot Number NS15881832X.

Where was it sold?

Worldwide distribution.

What should I do if I have it?

Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.

What does Class II mean?

Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.

Read the official FDA notice · Source record retrieved 26 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

Other products in this recall event

17 other products · FDA event 98495

This product is part of a recall event; the main page for the event is Medical Arterial Pressure Monitoring Tray, Reference recalled.

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