Washington recalls
4098 federal recalls on file affecting Washington - 719 Washington-specific plus 3379 nationwide. Sourced from CPSC, FDA, USDA, and NHTSA.
- 2026-02-18FDA-DeviceMedlineClass INationwideStop using Medline ReNewal ViewFlex Xtra ICE Catheters
These lots of reprocessed catheters may contain small particles of residual material. If affected devices are used, there is a risk of inflammatory response, systemic infection, or granulomatous reaction or thrombus reaction which may lead to cerebral or pulmonary embolism, or deep vein thrombosis. Expansion of recall Z-2610/2614-2025
- 2026-02-18FDA-DeviceMedlineClass INationwideStop using affected St. Jude Supreme catheters
These lots of reprocessed catheters may contain small particles of residual material. If affected devices are used, there is a risk of inflammatory response, systemic infection, or granulomatous reaction or thrombus reaction which may lead to cerebral or pulmonary embolism, or deep vein thrombosis. Expansion of recall Z-2610/2614-2025
- 2026-02-18FDA-DeviceMedlineClass INationwideStop using affected Medline Livewire catheters
These lots of reprocessed catheters may contain small particles of residual material. If affected devices are used, there is a risk of inflammatory response, systemic infection, or granulomatous reaction or thrombus reaction which may lead to cerebral or pulmonary embolism, or deep vein thrombosis. Expansion of recall Z-2610/2614-2025
- 2026-02-18FDA-DeviceMedlineClass INationwideReprocessed Abbott Inquiry Steerable Diagnostic Catheters: Abbott Inquiry Steerable Diagnostic Catheter 10 Elec. 2-5-2mm 81105RH 81172RH; Abbott Inquiry Steerable Diagnostic Catheter 20 Elec. 2-10-2mm 81202RH; Abbott Inquiry Steerable Diagnostic Catheter 4 Elec. 5mm 81483RH; Inquiry Steerable Diagnostic Catheter 10 Elec. 2-5-2mm 81102RH 81104RH 81174RH 81531RH 81532RH; Inquiry Steerable Diagnostic Catheter 10 Elec. 5mm 81107RH; Inquiry Steerable Diagnostic Cath
These lots of reprocessed catheters may contain small particles of residual material. If affected devices are used, there is a risk of inflammatory response, systemic infection, or granulomatous reaction or thrombus reaction which may lead to cerebral or pulmonary embolism, or deep vein thrombosis. Expansion of recall Z-2610/2614-2025
- 2026-02-18FDA-DeviceMedlineClass INationwideStop using Medline ReNewal Webster CS Catheters
These lots of reprocessed catheters may contain small particles of residual material. If affected devices are used, there is a risk of inflammatory response, systemic infection, or granulomatous reaction or thrombus reaction which may lead to cerebral or pulmonary embolism, or deep vein thrombosis. Expansion of recall Z-2610/2614-2025
- 2026-02-18FDA-DevicePhilipsClass IINationwideCheck your Philips Spectral CT 7500 fasteners
As part of the CT systems sub assembly, thirty-two (32) fasteners are used to attach the rotor to the bearing within the gantry. One or more of these fasteners may not be torqued to specification. If multiple fasteners are not torqued to specification, the rotor or rotor parts may become unsecured or displaced. While there has been no reported or observed event of expelled parts during gantry rotation, unsecured rotor parts may potentially be expelled.
- 2026-02-18FDA-DevicePhilipsClass IINationwideContact Philips about your Spectral CT system
As part of the CT systems sub assembly, thirty-two (32) fasteners are used to attach the rotor to the bearing within the gantry. One or more of these fasteners may not be torqued to specification. If multiple fasteners are not torqued to specification, the rotor or rotor parts may become unsecured or displaced. While there has been no reported or observed event of expelled parts during gantry rotation, unsecured rotor parts may potentially be expelled.
- 2026-02-18FDA-DevicePhilipsClass IINationwideContact Philips about your IQon Spectral CT
As part of the CT systems sub assembly, thirty-two (32) fasteners are used to attach the rotor to the bearing within the gantry. One or more of these fasteners may not be torqued to specification. If multiple fasteners are not torqued to specification, the rotor or rotor parts may become unsecured or displaced. While there has been no reported or observed event of expelled parts during gantry rotation, unsecured rotor parts may potentially be expelled.
- 2026-02-18FDA-DevicePhilipsClass IINationwideContact Philips about your Brilliance iCT scanner
As part of the CT systems sub assembly, thirty-two (32) fasteners are used to attach the rotor to the bearing within the gantry. One or more of these fasteners may not be torqued to specification. If multiple fasteners are not torqued to specification, the rotor or rotor parts may become unsecured or displaced. While there has been no reported or observed event of expelled parts during gantry rotation, unsecured rotor parts may potentially be expelled.
- 2026-02-18FDA-DeviceHologicClass IINationwideStop using Hologic Brevera biopsy needles
Presence of particulates in affected devices that can be deposited into breast tissue during use.
- 2026-02-18FDA-DeviceMedlineClass IINationwideStop using Medline Intubation Tray SKU DYNJAA245B
A smaller open suction catheter, the 8 Fr Suction Catheter, may have been packed within the kit instead of the required 14 Fr Suction Catheter. Use of the smaller size catheter may result in hypoxia and/or respiratory failure related to partial or full airway obstruction. Airway obstruction may require immediate emergent medical intervention to prevent respiratory failure or death. Other potential outcomes include prolonged procedure, airway irritation, or prolonged dyspnea.
- 2026-02-18FDA-DeviceMedlineClass IINationwideStop using Medline suction catheter kit DYND40972
A smaller open suction catheter, the 8 Fr Suction Catheter, may have been packed within the kit instead of the required 14 Fr Suction Catheter. Use of the smaller size catheter may result in hypoxia and/or respiratory failure related to partial or full airway obstruction. Airway obstruction may require immediate emergent medical intervention to prevent respiratory failure or death. Other potential outcomes include prolonged procedure, airway irritation, or prolonged dyspnea.
- 2026-02-18FDA-FoodMcCainClass IIStop using McCain Foods Sonic Tots
Foreign material (small hard plastic fragments).
- 2026-02-18FDA-FoodMcCainClass IIDon't serve Ore-Ida Tater Tots item OIF00215A
Foreign material (small hard plastic fragments).
- 2026-02-18FDA-FoodCostcoClass IDon't eat Kirkland Signature Mini Beignets
Undeclared hazelnut.
- 2026-02-18FDA-DrugMcKessonClass INationwideCheck your UDENYCA injection lot and serial number
Temperature Abuse. 116 cartons with specific serial numbers of Lot 2199821, were stored incorrectly in a controlled room temperature environment instead of the required refrigerated environment.
- 2026-02-18FDA-DrugMeitheal PharmaceuticalsClass IINationwideStop using Meitheal Cetrorelix Acetate injection kits
Defective Delivery System: Missing or duplicated needles within the injection kit
- 2026-02-18FDA-DrugAmerisourceClass IINationwideCheck your oxycodone tablets for loose packaging
Defective container: card seal defects (weak/non-existent seals), leading to the tablets falling out of their cavities.
- 2026-02-18FDA-DrugFresenius KabiClass IINationwideStop using recalled Fresenius Kabi vancomycin injection
Lack of Assurance of Sterility
- 2026-02-18FDA-DrugFresenius KabiClass IINationwideStop using Fresenius Kabi vancomycin HCl IV bags
Lack of Assurance of Sterility
- 2026-02-18FDA-DrugFresenius KabiClass IINationwideDo not use Fresenius Kabi thiamine HCl injection
Lack of Assurance of Sterility
- 2026-02-18FDA-DrugFresenius KabiClass IINationwideDo not use Fresenius Kabi ketamine HCl injection
Lack of Assurance of Sterility
- 2026-02-18FDA-DrugFresenius KabiClass IINationwideDo not use Fresenius Kabi acyclovir sodium IV bags
Lack of Assurance of Sterility
- 2026-02-18FDA-DrugAsteria HealthClass IINationwideStop using Asteria Health testosterone pellets
Presence of Foreign substance - potential presence of metal particulate matter
- 2026-02-18FDA-DrugAsteria HealthClass IINationwideStop using Asteria Health testosterone pellets
Presence of Foreign substance - potential presence of metal particulate matter
- 2026-02-18FDA-DrugAsteria HealthClass IINationwideStop using Asteria Health hormone pellets
Presence of Foreign substance - potential presence of metal particulate matter
- 2026-02-18FDA-DrugAsteria HealthClass IINationwideStop using Asteria Health hormone pellets
Presence of Foreign substance - potential presence of metal particulate matter
- 2026-02-18FDA-DrugAsteria HealthClass IINationwideStop using Asteria Health testosterone pellets
Presence of Foreign substance - potential presence of metal particulate matter
- 2026-02-18FDA-DrugAsteria HealthClass IINationwideStop using Asteria Health testosterone pellets
Presence of Foreign substance - potential presence of metal particulate matter
- 2026-02-18FDA-DrugAsteria HealthClass IINationwideStop using Asteria Health testosterone pellets
Presence of Foreign substance - potential presence of metal particulate matter
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