Fresh Recalls

FDAClass II · Medical device · Recall Z-2930-2026 · Recalled August 19, 2026

GLIDESHEATH SLENDER A-KIT 6F 10CM recall — Terumo Medical Corporation

Agency report date: August 19, 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
GLIDESHEATH SLENDER A-KIT 6F 10CM
Company / brand
Terumo Medical
Lot / serial / date codes
Product Code: 60-1060. Shelfbox UDI-DI: 30389701011975; Pouch UDI-DI: 00389701011974; UDI-PI: (17)280501(10)0001441871. Lot Number: 0001441871.
Distribution
Worldwide distribution - US Nationwide and the country of Canada.
Agency product description and boundaries

GLIDESHEATH SLENDER A-KIT 6F 10CM .021GW. 5 units per box. Product Code: 60-1060. The Glidesheath Slender is used to facilitate placing a catheter through the skin into the radial artery.

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: Product was packaged with the 0.025 guidewire instead of the 0.021 guidewire.

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: GLIDESHEATH SLENDER A-KIT 6F 10CM

3. Open the official notice or contact

Official recall ID
Z-2930-2026
Brand
Terumo Medical
Classification
Class II
Units affected
7,490 units
Recall status
Ongoing
Initiated
Voluntary: Firm initiated

Affected products

Companies & origin

Recalling firm location
Elkton, MD, United States
Firm address
950 Elkton Blvd, 21921-5322

Identifying details (verbatim from the notice)

Product codes / lots
Product Code: 60-1060. Shelfbox UDI-DI: 30389701011975; Pouch UDI-DI: 00389701011974; UDI-PI: (17)280501(10)0001441871. Lot Number: 0001441871.
Distribution
Worldwide distribution - US Nationwide and the country of Canada.
Firm notified the public via
Two or more of the following: Email, Fax, Letter, Press Release, Telephone, Visit
FDA event ID
99285
Recall initiated
June 15, 2026
FDA classified
August 10, 2026
FDA report date
August 19, 2026
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 September 7, 2026 at 6:00 AM UTC. Record retrieved September 7, 2026 at 6:00 AM UTC.

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