Fresh Recalls

FDAClass II · Medical device · Recall Z-0117-2027 · Recalled October 14, 2026

TufTex¿ Over-the-Wire Embolectomy Catheter recall — LeMaitre Vascular, Inc.

Agency report date: October 14, 2026.

1. Compare your item

This notice names a product; your particular item is not yet verified. Compare every applicable model, serial, lot, production-date or model-year boundary below.

Product named
TufTex¿ Over-the-Wire Embolectomy Catheter
Company / brand
LeMaitre Vascular
Lot / serial / date codes
Catalog Number: E1651-88; UDI-DI: 00840663100866; Lot Number: XOT00002181;
Distribution
US Nationwide distribution in the states of CA, FL, GA, KY, LA, NJ, OH, PA, SC.
Agency product description and boundaries

TufTex¿ Over-the-Wire Embolectomy Catheter; Catalog Number: E1651-88;

Still to verify: match the label on your item with the full official notice, including any exclusions, tables and photos. Some identifiers appear only on the agency website and are absent from this data feed. A missing field does not mean all versions are affected.

If your lot or date falls outside a stated range, this notice has not established that your item is affected. This is not a finding about other recalls or product safety.

2. Agency hazard and consumer action

FDA reports: Devices failed in process testing related to the amount of pull force it can sustain prior to the balloon components failing.

No consumer remedy instructions are supplied in this record. Check the official notice and listed company contact for the agency’s current instructions.

Class II: may cause temporary or medically reversible health consequences.

Affected product: TufTex¿ Over-the-Wire Embolectomy Catheter recall status

3. Open the official notice or contact

Official recall ID
Z-0117-2027
Brand
All LeMaitre Vascular recalls
Classification
Class II
Units affected
54
Recall status
Ongoing
Initiated
Voluntary: Firm initiated

Affected products

Companies & origin

Recalling firm location
Burlington, MA, United States
Firm address
32 3rd Ave, N/A, 01803-4414

Identifying details (verbatim from the notice)

Product codes / lots
Catalog Number: E1651-88; UDI-DI: 00840663100866; Lot Number: XOT00002181;
Distribution
US Nationwide distribution in the states of CA, FL, GA, KY, LA, NJ, OH, PA, SC.
Firm notified the public via
Letter
FDA event ID
99836
Recall initiated
August 28, 2026
FDA classified
October 7, 2026
FDA report date
October 14, 2026

Other medical device recalls from around the same time

Verify with the official sources:

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Source: U.S. Food & Drug Administration. Agency excerpts come from the public data feed and may omit tables or later changes; the linked government source is authoritative. Source last checked October 22, 2026 at 12:00 PM UTC. Record retrieved October 22, 2026 at 12:00 PM UTC.

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