Recall archive / FDA device enforcement
Roadrunner UniGlide Hydrophilic Wire Guide REFERENCE PART NUMBER (RPN): HPWA-35-150 ORDER NUMBER (GPN): G56173. For v... — FDA record Z-1713-2022
Reported ongoing
Status as reported in the agency record. FDA warns that enforcement status may not track the current recall lifecycle; check the current official notice.
Source date Jul 19, 2022. Retrieved Oct 1, 2026. Last updated Oct 1, 2026.
Archive changed Oct 1, 2026. USDA FSIS records are unavailable; check FSIS directly. Source coverage and dates.
What the record says
- Product
- 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.
- Reason
- 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.
- Classification
- Class II
- Recalling firm
- Cook Incorporated
- Quantity
- 5400 units
- Agency-reported status
- Ongoing
- Source record identifier
- Z-1713-2022
What the recall classes mean. Classification is an agency assessment, not individual medical advice.
Lot and product identifiers
| Label field | Details supplied by the agency |
|---|---|
| Lot, code or applicability | 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 |
Match all identifying details in the current notice. A brand name alone is not enough.
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
States below are derived from the distribution text, including nationwide wording. They are not inferred from the firm's address.
- Alaska
- Alabama
- Arkansas
- Arizona
- California
- Colorado
- Connecticut
- Delaware
- Florida
- Georgia
- Hawaii
- Iowa
- Idaho
- Illinois
- Indiana
- Kansas
- Kentucky
- Louisiana
- Massachusetts
- Maryland
- Maine
- Michigan
- Minnesota
- Missouri
- Mississippi
- Montana
- North Carolina
- North Dakota
- Nebraska
- New Hampshire
- New Jersey
- New Mexico
- Nevada
- New York
- Ohio
- Oklahoma
- Oregon
- Pennsylvania
- Rhode Island
- South Carolina
- South Dakota
- Tennessee
- Texas
- Utah
- Virginia
- Vermont
- Washington
- Wisconsin
- West Virginia
- Wyoming
Dates in the source
- Report date
- Sep 21, 2022
- Recall initiation date
- Jul 19, 2022
- Center classification date
- Sep 9, 2022
FDA company pages use the listing date; enforcement records use initiation dates; CPSC uses recall date; NHTSA uses report-received date. These dates are not interchangeable.