Galt Medical Corporation recalls
Every recall we track for Galt Medical Corporation — 19 in all, from 2018–2026 — plus the complaints and injury reports the public filed about them.
Recalls per year, by danger level
Recalls from Galt Medical Corporation peaked in 2018 (8); 19 since 2017.
All FDA recall records for Galt Medical Corporation since 2017, counted by recall date (one bar per calendar year; 2026 is partial). Danger level is GovInfoNow’s plain-language rating; “not yet rated” records are still being written up.
| Year | Stop using now | Use caution | Lower risk | Not yet rated | Total |
|---|---|---|---|---|---|
| 2017 | 0 | 0 | 0 | 0 | 0 |
| 2018 | 0 | 2 | 5 | 1 | 8 |
| 2019 | 0 | 0 | 0 | 0 | 0 |
| 2020 | 0 | 0 | 1 | 0 | 1 |
| 2021 | 0 | 0 | 0 | 0 | 0 |
| 2022 | 0 | 0 | 0 | 0 | 0 |
| 2023 | 0 | 0 | 2 | 0 | 2 |
| 2024 | 0 | 0 | 0 | 0 | 0 |
| 2025 | 0 | 0 | 7 | 0 | 7 |
| 2026 (to date) | 0 | 1 | 0 | 0 | 1 |
Most common reasons for Galt Medical Corporation recalls
What to do if you have a recalled Galt Medical Corporation product
- Match the model, catalog or lot number on your device to the recall.
- Ask the prescribing clinician or supplier what to do — many device recalls are corrections, not removals.
- Report problems to FDA MedWatch.
All Galt Medical Corporation recalls
5 shown- Use cautionMedical device
Galt Medical Corporation recalls Boston Scientific Enhance Transcarotid/Peripheral Access Kit REF: SR-4F21G7D-MP (Kit-075-03) Sheath with Dilator ,
Boston Scientific recalls transcarotid access kits with potential depth markings that may detach from sheath, causing injury during medical procedures.
Boston ScientificJun 26, 2026 - Lower riskMedical device
Galt Medical Corporation recalls GALT Guidewire REF SGW-051-07 Guidewires are intended for use in percutaneous procedures, to introduce and position
Galt Medical recalls GALT Guidewire REF SGW-051-07 due to potential open seal in sterile packaging. This could compromise sterility during medical procedures.
Galt MedicalMar 27, 2025 - Lower riskMedical device
Galt Medical Corporation recalls Tearaway Introducer Kit, REF: KIT-010-12, KIT-010-17, KIT-900-16
Galt Medical recalls Tearaway Introducer Kits with serial numbers KIT-010-12, KIT-010-17, KIT-900-16 due to potential luer connection cracks causing dilator hub dislodgement. Affected kits may require replacement.
Galt MedicalMay 8, 2023 - Lower riskMedical device
Galt Medical Corporation recalls Centeze Centesis Catheter, 6F, 10cm, 18Ga, 12cm, REF DRC-002-06 Centeze Centesis Catheter, 6F, 10cm, 18Ga, 12cm, REF
Galt Medical recalls specific Centeze catheter models due to incorrect tip geometry causing potential blockage. Affected units include certain lot numbers and catalog codes from 2010-2023.
Galt MedicalNov 16, 2020 - Use cautionMedical device
Galt Medical Corporation recalls 1) Drainer Centesis Catheter, Sterile EO, Rx Only, Catalog #: a) DRC-001-05, b) DRC-001-06, c) DRC-001-15, 2) Centeze
Galt Medical recalls specific Drainer Centesis Catheters (catalog numbers DRC-001-05 to DRC-001-15 and DRC-002-02 to DRC-002-08) due to potential unsafe bacterial endotoxin levels that could cause fever, chills, and low blood pressure.
Galt MedicalMay 2, 2018
Galt Medical Corporation recall questions
How many recalls has Galt Medical Corporation had?
19 recalls from Galt Medical Corporation are on record with U.S. safety agencies, from 2018–2026.
What is the most recent Galt Medical Corporation recall?
Galt Medical Corporation recalls Boston Scientific Enhance Transcarotid/Peripheral Access Kit REF: SR-4F21G7D-MP (Kit-075-03) Sheath with Dilator ,, dated Jun 26, 2026. Every Galt Medical Corporation recall is listed on this page, newest first.
Why are Galt Medical Corporation products recalled?
The most common reasons on record: Due to a potential open seal in the sterile barrier packaging. (4); Due to a potential open seal in the sterile barrier packaging . (3).
What should I do if I have a recalled Galt Medical Corporation product?
Match the model, catalog or lot number on your device to the recall. Ask the prescribing clinician or supplier what to do — many device recalls are corrections, not removals. Report problems to FDA MedWatch.
How do I get alerts for new Galt Medical Corporation recalls?
Sign up for free email alerts on GovInfoNow — we check official CPSC, FDA, USDA and NHTSA data every day and email you only when a recall matches what you follow.