Terumo Medical recall: Glidesheath Slender a-Kit 6F 10CM .021GW
Terumo Medical Corporation is recalling Glidesheath Slender a-Kit 6F 10CM .021GW – 7,490 units. The U.S. Food and Drug Administration published the recall on August 19, 2026; it began on June 15, 2026. Distributed nationwide.
Serious Class II means the product may cause temporary or medically reversible health problems, or the chance of serious harm is remote.
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| Product | Glidesheath Slender a-Kit 6F 10CM .021GW |
| Brand | Terumo Medical |
| Company | Terumo Medical Corporation |
| Type | Medical devices |
| Classification | Class II |
| Recall date | June 15, 2026 |
| Published by FDA | August 19, 2026 |
| Quantity | 7,490 units |
| Recall ID | 99285 |
Recalled products
- 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.
- FDA recall number
- Z-2930-2026
- Codes, lots and dates
- Product Code: 60-1060. Shelfbox UDI-DI: 30389701011975; Pouch UDI-DI: 00389701011974; UDI-PI: (17)280501(10)0001441871. Lot Number: 0001441871.
- Quantity
- 7,490 units
- Classification
- Class II
Identifiers and details
- FDA event ID
- 99285
- Initiated
- Voluntary: Firm initiated
- Status
- Ongoing
- Firm location
- Elkton, MD, United States
Why it was recalled
The reason the FDA lists: “Product was packaged with the 0.025 guidewire instead of the 0.021 guidewire.”
Where it was sold
Nationwide. Distribution as the FDA records it: “Worldwide distribution - US Nationwide and the country of Canada.”
What to do
Compare the recall numbers, lot numbers and expiration dates with what you have. Do not stop a prescribed medicine or device without talking to your pharmacist or doctor – they can arrange a replacement from an unaffected lot.
Official notice: FDA Enforcement Report record (event 99285, openFDA) – the same recall numbers can be searched in the FDA Enforcement Report.
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|---|---|---|---|
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| Oct 7, 2026 | Karl Storz Endoscopy recall: HOPKINS Telescope 30¿Medical devices · 6 eyepieces | Due to incorrect inside packaging label for eyepiece. Serious | FDA Class II |
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| Oct 7, 2026 | Siemens Healthcare Diagnostics recall: Atellica CH Revised C-Reactive ProteinMedical devices · 42940 units (3938 US, 39002 OUS) | The potential for falsely elevated results. Serious | FDA Class II |
| Oct 7, 2026 | Tandem Diabetes Care recall: T:slim Mobile ApplicationMedical devices · 177 | A beta (early-release) version of the iOS application, version 2.13 (TestFlight) had a sof… Serious | FDA Class II |
About this recall
Is Terumo Medical Glidesheath Slender a-Kit 6F 10CM .021GW recalled?
Yes. Terumo Medical Corporation recalled it on June 15, 2026; FDA published it August 19, 2026 (Class II). Only the lots, dates or models listed on this page are included.
Why was it recalled?
Product was packaged with the 0.025 guidewire instead of the 0.021 guidewire.
What should I do if I have it?
Compare the recall numbers, lot numbers and expiration dates with what you have. Do not stop a prescribed medicine or device without talking to your pharmacist or doctor – they can arrange a replacement from an unaffected lot.
Where was it sold?
Nationwide.
More recalls
Source: recall records published by the U.S. Food and Drug Administration (openFDA Enforcement Reports), the USDA Food Safety and Inspection Service, the Consumer Product Safety Commission and the National Highway Traffic Safety Administration, collected twice a day. Product names, lot codes, dates and model numbers are shown exactly as the agency lists them; the agency's notice is the authority. 77.today is not affiliated with any of these agencies.