CLASS II ONGOING Device recall · Reported 1 Feb 2023 · FDA Enforcement Report

Centurion Medical Products, Silver Antimicrobial Vad Drive recalled

Medline Industries LP - Northfield is recalling Centurion Medical Products, Silver Antimicrobial Vad Drive, distributed nationwide in the US. The recall was initiated on 23 Dec 2022 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesUDI/DI 10653160274841, Lot Numbers 22ABO498

Quantity recalled1050 kits

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-1015-2023
FDA event ID: 91420
Recalling firm: Medline Industries LP - Northfield, Northfield, IL
Classification: Class II
Status: Ongoing
Recall initiated: 23 Dec 2022
FDA classified: 25 Jan 2023
Reported: 1 Feb 2023
Type: Voluntary: Firm initiated
Customers notified by: Letter
Reason category: Other Reasons
Device type: Other Medical Devices

Timeline

23 Dec 2022	Recall initiated by company
25 Jan 2023	Classified by FDA	+33 days
1 Feb 2023	Published in enforcement report	+7 days

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

Reason for recall

The kit contained an expired component.

Product as listed by the FDA

CENTURION MEDICAL PRODUCTS, SILVER ANTIMICROBIAL VAD DRIVE, REF DT18760

Where it was distributed

US Nationwide distribution in the states of NY, IN, FL, NJ, IL.

Nationwide Florida Illinois Indiana New Jersey New York

Questions about this recall

Why was it recalled?

The kit contained an expired component.

Which lots are affected?

UDI/DI 10653160274841, Lot Numbers 22ABO498

Where was it sold?

US Nationwide distribution in the states of NY, IN, FL, NJ, IL.

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.

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