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PILLING

TELEFLEX INCORPORATED · Model IPN018606 · UDI-DI 34026704651796

DXC Prescription
10
510(k) clearances
12,981
Adverse events (78 deaths)
26
Recalls
182
Facilities

Description

CLAMP NEONATAL VASC COOLEY CAROTID 5"

Recalls

DateFirmReason
2025-08-15Maquet Cardiovascular, LLCThree failure modes have been identified: failure of the Heartstring Seal to load, failure of the Heartstring Seal to deploy into the aortotomy, and failure of the deployed Heartst
2025-08-15Maquet Cardiovascular, LLCThree failure modes have been identified: failure of the Heartstring Seal to load, failure of the Heartstring Seal to deploy into the aortotomy, and failure of the deployed Heartst
2025-08-15Maquet Cardiovascular, LLCThree failure modes have been identified: failure of the Heartstring Seal to load, failure of the Heartstring Seal to deploy into the aortotomy, and failure of the deployed Heartst
2025-07-01North American Rescue LLC.Device used for unilateral or bilateral occlusion of blood flow to the lower limbs has a potential manufacturing defect that may compromise the structural integrity of the device a
2024-02-22Baxter Healthcare CorporationThe Surgical Tools and Cardiovascular Specialty marketing brochures distributed for Flo-Rester Disposable Internal Vessel Occluder, Flo-Thru Intraluminal Shunt, and Vascular Probe
2024-02-22Baxter Healthcare CorporationThe Surgical Tools and Cardiovascular Specialty marketing brochures distributed for Flo-Rester Disposable Internal Vessel Occluder, Flo-Thru Intraluminal Shunt, and Vascular Probe
2024-02-22Baxter Healthcare CorporationThe Surgical Tools and Cardiovascular Specialty marketing brochures distributed for Flo-Rester Disposable Internal Vessel Occluder, Flo-Thru Intraluminal Shunt, and Vascular Probe
2023-12-06Baxter Healthcare CorporationCardiovascular Surgery marketing brochure (US-AS46-220001) that was distributed for the products listed below contains inaccurate content that does not align with some of the produ
2023-12-06Baxter Healthcare CorporationCardiovascular Surgery marketing brochure (US-AS46-220001) that was distributed for the products listed below contains inaccurate content that does not align with some of the produ
2022-04-01Baxter Healthcare CorporationThere is a potential for foreign matter.

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Data compiled from public U.S. FDA sources (GUDID, 510(k)/PMA, MAUDE, recalls, establishment registration). Adverse-event reports are unverified and do not establish causation. Informational only — not medical, clinical, or regulatory advice.