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FDA (Device enforcement)Recalled 2022-07-19class ii

Cook Incorporated: Roadrunner UniGlide Hydrophilic Wire Guide REFERENCE PART NUMBER (RPN): HPWA-35-150 ORDER NUMBER (GPN): G56173. For vascular catheter positioning and exchange in diagnostic and inte

Is my product affected?

Roadrunner UniGlide Hydrophilic Wire Guide REFERENCE PART NUMBER (RPN): HPWA-35-150 ORDER NUMBER (GPN): G56173. For vascular catheter positioning and exchange in diagnostic and interventional procedures.

  • UPC 00827002561731

Check against the official notice below — it lists the full affected range.

What happened

Cook Incorporated is recalling the Roadrunner UniGlide Hydrophilic Wire Guide (Part Number HPWA-35-150, Order Number G56173), a device used for vascular catheter positioning and exchange. The recall affects 5,400 units distributed nationwide and internationally across multiple countries. The product failed packaging testing requirements, including 3-year age acceleration testing, which means the sterility of the device may be compromised.

The affected devices were distributed under specific lot numbers ranging from 14070910 through NS14176970. The source document does not specify a remedy or recommended course of action for consumers who may have affected units.

Written by software from the official notice below. Not reviewed by a lawyer.

Hazard

Product did not meet the acceptance criteria for packaging testing, which included 3-year age acceleration testing, therefore, the sterility of the device may be compromised.

Details from the source

Reason for recall: Product did not meet the acceptance criteria for packaging testing, which included 3-year age acceleration testing, therefore, the sterility of the device may be compromised. Distribution: Nationwide Foreign: AR AT AU BE BG CA CA CH CL CN CZ DE DK ES FR GB GR GU HU IL IT JO JP KR KW MX MY NC NL PE PL PR PT PY RU SE SI TR UY ZA Quantity: 5400 units Lot/code info: UDI-DI: (01)00827002561731- Lot Numbers: 14070910, 14070913, 14070914, 14070915, 14070916, 14070917, 14080810, 14104898, 14104899, 14104902, 14106628, 14106629, 14120473, 14120474, 14120475, 14122089, 14122091, 14122093, 14122095, 14122322, 14129155, 14129156, 14129157, 14129158, 14129161, 14129162, 14129163, 14131012, 14131013, 14131014, 14134680, 14134681, 14134683, 14134684, 14139356, 14142001, 14142004, 14142005, 14142007, 14147337, 14147338, 14147339, 14148371, 14160531, 14160533, 14160534, NS14095649, NS14122100, NS14122327, NS14129168, NS14131010, NS14131011, NS14131015, NS14133505, NS14142008, NS14147334, NS14147335, NS14147336, NS14147336X, NS14153793, NS14176970

Source

Official record: FDA (Device enforcement) ↗

Republished from the official source above; details can change — the source record controls.

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