CLASS II ONGOING Device recall · Reported 4 Feb 2026 · FDA Enforcement Report

Brand Name: LimFlow Vector Product Name recalled

LimFlow is recalling LimFlow Vector, distributed nationwide in the US. The recall was initiated on 5 Dec 2025 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesLot Code: Model: VT-US-23 Lot: 82321838 GTIN: 00850041730134 U.S. Product Code: MGZ

Quantity recalled33 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-1218-2026
FDA event ID: 98218
Recalling firm: LimFlow, San Jose, CA
Classification: Class II
Status: Ongoing
Recall initiated: 5 Dec 2025
FDA classified: 29 Jan 2026
Reported: 4 Feb 2026
Type: Voluntary: Firm initiated
Customers notified by: Letter
Reason category: Other Reasons
Device type: Other Medical Devices

Timeline

5 Dec 2025	Recall initiated by company
29 Jan 2026	Classified by FDA	+55 days
4 Feb 2026	Published in enforcement report	+6 days

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

Reason for recall

Incorrect expiration date

Product as listed by the FDA

Brand Name: LimFlow Vector Product Name: LimFlow Vector Model/Catalog Number: VT-US-23

Where it was distributed

US Nationwide distribution in the states of AL, CT, District of Columbia, FL, KY, MA, MI, NE, NJ, NY, OH, PA, RI, TX, WY.

Nationwide Alabama Connecticut District of Columbia Florida Kentucky Massachusetts Michigan Nebraska New Jersey New York Ohio Pennsylvania Rhode Island Texas Wyoming

Questions about this recall

Is Brand Name: LimFlow Vector Product Name: LimFlow Vector Model/Catalog recalled?

Yes. LimFlow recalled Brand Name: LimFlow Vector Product Name: LimFlow Vector Model/Catalog on 5 Dec 2025. The recall is Class II and its status is Ongoing. Recall number Z-1218-2026.

Why was it recalled?

Incorrect expiration date

Which lots are affected?

Lot Code: Model: VT-US-23 Lot: 82321838 GTIN: 00850041730134 U.S. Product Code: MGZ

Where was it sold?

US Nationwide distribution in the states of AL, CT, District of Columbia, FL, KY, MA, MI, NE, NJ, NY, OH, PA, RI, TX, WY.

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 21 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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