State

Washington product recalls

73,817 recalls have nationwide distribution and so reach Washington. 8,536 additional recalls listed Washington specifically in their distribution scope.

What the numbers show

Total: 8,536
Critical: 865
Severe: 2,405
Most recent: 2026-11-04

Of the 8,536 recalls naming Washington we have scored against our rubric, 865 (10%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,405 (28%) are Severe.

Which agencies issued them

These figures cover only the 8,536 recalls whose distribution notice names Washington specifically. The 73,817 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

43301–43325 of 82353

SevereFDA (Food)·F-1011-2018·2018-04-18
Bob's Red Mill Organic Amaranth Flour Recalled for Salmonella Risk
Bob's Red Mill Natural Foods is recalling Organic Whole Grain Amaranth Flour due to potential Salmonella contamination. The product was distributed in ten US states, Mexico, and the UAE.
Product
Amaranth Flour, Organic Whole Grain, Item Number: 6001C224, Net wt. 22 oz. UPC 0 39978 00911 1. The label is read in parts: "***Bob's Red Mill ***ORGANIC WHOLE GRAIN AMARANTH FLOUR STONE GROUND*** NET WT 22 OZ ***keeps best refrigerated or frozen***".
Category
Food
Distribution
11 states
SevereFDA (Devices)·Z-1365-2018·2018-04-18
Fresenius Liberty Select Cycler Recalled for Software Overfill Risk
Fresenius Medical Care is recalling Liberty Select Cyclers due to a software issue that may cause overfill, posing a risk of serious injury or death.
Product
Liberty Select Cycler (SW v.2.8.7), Material Number RTLR108343 Product Usage: The device is indicated for acute and chronic peritoneal dialysis.
Category
Medical Device
Distribution
Distributed nationwide
SevereNHTSA·18V247000·2018-04-18
Volkswagen Recalls 2006-2007 Passat Vehicles Due to Air Bag Inflator Defect
Volkswagen is recalling 2006-2007 Passat sedans and wagons because the driver's air bag inflator may explode during deployment, posing a risk of serious injury or death.
Product
VOLKSWAGEN — VOLKSWAGEN PASSAT, PASSAT WAGON
Category
Vehicle
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1351-2018·2018-04-18
W & H DentalWerk Recalls S-N1 and S-N2 Foot Controls
W & H DentalWerk is recalling S-N1 and S-N2 foot controls because they may fail to stop the motor, posing a risk of serious patient injury.
Product
Foot Controls Model: S-N1 and S-N2 Product Usage: Variable foot control for use with drive units operating mechanical instruments.
Category
Medical Device
Distribution
Distributed nationwide
SevereFDA (Devices)·Z-1318-2018·2018-04-18
Reliance Medical Products Recalls Refractor Suspension Arms Due to Missing Parts
Reliance Medical Products is recalling 933 Refractor Suspension Arms because missing parts caused the device to fall on a patient.
Product
Refractor Suspension Arm (P/N: 525004, 05 and 525006, 07) The Intended use of this medical device, as part of system to store and position ophthalmological examination and diagnostic equipment, is to store and position for examination a device commonly known as a…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-1141-2018·2018-04-18
Poppies International Recalls Belgian Mini Eclairs Due to Listeria Risk
Poppies International is recalling three brands of frozen Belgian mini eclairs because they may be contaminated with Listeria monocytogenes.
Product
GFS Belgian Mini Chocolate Topped Eclairs, Keep Frozen, Net Wt . 700 g.; Signature Select Belgian Style Mini Eclairs, Keep Frozen, 420 g; Delizza Patisserie Belgian Custard Cream Mini Eclairs, 420 g.
Category
Food
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1320-2018·2018-04-18
Mindray Hematology Diluent M-30D Recalled for Elevated Platelet Background Counts
Mindray is recalling specific lots of M-30D diluent used with BC-3200 and BC-3600 analyzers because they may cause the system to produce an elevated platelet background count.
Product
Hematology Diluent M-30D used with BC-3200 and BC-3600 Hematology Analyzer; Part Numbers: (1) 105-005405-00 (2 x 5.5L container), (2) 105-005406-00 (20L container) The M-30D Diluent is an azide-free, filtered isotonic solution for counting and sizing blood cells. It is for…
Category
Medical Device
Distribution
6 states
HighFDA (Devices)·Z-1344-2018·2018-04-18
ICU Medical Recalls 7-inch Intravascular Administration Sets with Incorrect Spin Collar
ICU Medical is recalling 250 pouches of 7-inch intravascular administration sets because they were manufactured with an incorrect spin collar.
Product
7" Ext Set w/MicroClave¿, Clave¿ T-Connector, Clamp, Rotating Luer, 50 pouches per case, Item AH7262. The firm name on the label is icumedical, San Clemente, CA. The Intravascular Administration Set is a single use, sterile, non-pyrogenic device which provides access for…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1372-2018·2018-04-18
Hamilton-C3 Ventilator Battery Fuel Gauge Recall
Hamilton Medical AG is recalling 739 Hamilton-C3 Ventilator Units worldwide because the battery fuel gauge may inaccurately indicate a higher charge than available.
Product
Hamilton-C3 Ventilator Unit Intended to provide ventilator support to adults and pediatrics and optionally infants and neonates in the hospital.
Category
Medical Device
Distribution
29 states
HighFDA (Devices)·Z-1367-2018·2018-04-18
Teleflex Medical Recalls Latex Rebreathing Bags Due to Missing Allergen Warning
Teleflex Medical Europe Ltd is recalling 107,962 latex rebreathing bags because they lack the required warning that the product contains natural rubber latex, which may cause allergic reactions.
Product
Latex Rebreathing Bags: Product Code Equivalent Code (a) 151174050 151174 (b) 153000005 153000005 (c) 153000010 153000010 (d) 153000020 153000020 (e) 153000030 153000030 (f) 153000050 153000050 (g) 210700050 2107050 (h) 210700102 2107102 (I) 210700202 2107202 (j)…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1356-2018·2018-04-18
Bard Feeding Tubes Recalled for Ineffective Connector Fusion
C.R. Bard is recalling specific lots of Bard Adult/Pediatric Feeding Tubes because the tubing and ENFit connector may not be fused effectively.
Product
Bard(R) Adult/Pediatric Feeding Tube, ENFit(TM), REF EN0036420 Product Usage: BARD(R) Nasogastric Sump Tubes with ENFit(TM) connector are intended to be used for: Decompression of stomach by suction or aspiration of gastric contents Short-term administration of term…
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·18V245000·2018-04-18
Newmar Recalls Motorhomes Due to Headlight Beam Switching Defect
Newmar is recalling specific 2013-2017 motorhomes because low beam headlights turn off when high beams are activated, reducing driver visibility.
Product
NEWMAR — NEWMAR LONDON AIRE, DUTCH STAR, VENTANA
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1349-2018·2018-04-18
Getinge Recalls VOLISTA StandOP Surgical Lights Due to Handle Detachment Risk
Getinge is recalling 5,214 VOLISTA StandOP surgical lights because the central handle holder can detach, potentially dropping particles into the sterile field during procedures.
Product
VOLISTA StandOP Surgical Light; Model numbers VLT600 SF AIM STP, VLT600 DF AIM STP, Ref. codes ARD568811901, ARD568811911 ARD568811951, ARD568811961 The device is designed to illuminate the body of a patient during surgical operations, diagnostics and treatment. These…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1355-2018·2018-04-18
Bard Infant Feeding Tube Recalled for Ineffective Connector Fusion
C.R. Bard is recalling 23,400 infant feeding tubes because the tubing and connector may not be effectively fused.
Product
Bard(R) Infant Feeding Tube, ENFit(TM), REF EN0036410 Product Usage: BARD(R) Nasogastric Sump Tubes with ENFit(TM) connector are intended to be used for: Decompression of stomach by suction or aspiration of gastric contents Short-term administration of term tube…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1341-2018·2018-04-18
Beckman Coulter AQUIOS CL Flow Cytometer System Recalled for Sample ID Errors
Beckman Coulter is recalling 288 AQUIOS CL Flow Cytometer Systems because the single tube loader may process the same sample with two different IDs, potentially causing erroneous results.
Product
AQUIOS CL Flow Cytometer System, Catalog #B30166. The AQUIOS CL Flow Cytometer system is an automated analyzer that use a no-wash sample preparation process.The firm name on the label is Beckman Coulter Ireland, Inc., Co. Clare, Ireland.
Category
Medical Device
Distribution
Distributed nationwide
HighCPSC·18142·2018-04-18
Primark Recalls Decorative Cushions Due to Fire Hazard
Primark is recalling about 14,500 decorative cushions sold in the northeastern U.S. because they can catch fire if exposed to an ignition source.
Product
Decorative cushions
Category
Consumer Product
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1319-2018·2018-04-18
Hill-Rom Progressa Bed Recall Due to Brake Component Failure Risk
Hill-Rom is recalling 2,117 Progressa adjustable hospital beds because a braking system component may break, causing unwanted bed movement and potential injury.
Product
Progressa Bed - AC-powered adjustable hospital bed
Category
Medical Device
Distribution
Distributed nationwide
HighNHTSA·18V246000·2018-04-18
Riverside Recalls 2015-2017 Motorhomes Due to Fire Extinguisher Defects
Riverside RV is recalling 2015-2017 White Water, Water Fall, and Mt. McKinley motorhomes because certain fire extinguishers may clog or detach, posing injury risks.
Product
RIVERSIDE — RIVERSIDE WATER FALL, MT. MCKINLEY, WHITEWATER
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1357-2018·2018-04-18
Bard Premature Infant Feeding Tubes Recalled for Ineffective Fusion
C.R. Bard is recalling specific lots of Bard Premature Infant Feeding Tubes because the tubing and ENFit connector may not be effectively fused.
Product
Bard(R) Premature Infant Feeding tube, ENFit(TM), REF EN0036430 Product Usage: BARD(R) Nasogastric Sump Tubes with ENFit(TM) connector are intended to be used for: Decompression of stomach by suction or aspiration of gastric contents Short-term administration of term…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Food)·F-1007-2018·2018-04-18
Taylor Shellfish Recalls Original Smoked Oysters Due to Packaging Error
Taylor Shellfish Co is recalling Original Smoked Oysters in vacuum pouches because the packaging method is incorrect for this product type, posing a potential botulism risk if not kept cold.
Product
Original Smoked Oysters, packaged in vacuum pouches, net wt. 2.25 oz. or 16 oz.. UPC 47094 20002
Category
Food
Distribution
2 states
HighFDA (Devices)·Z-1371-2018·2018-04-18
Hamilton-C2 Ventilator Units Recalled Due to Battery Fuel Gauge Inaccuracy
Hamilton Medical AG is recalling 739 Hamilton-C2 Ventilator Units worldwide because the battery fuel gauge may inaccurately indicate a higher charge than available.
Product
Hamilton-C2 Ventilator Unit Intended to provide ventilator support to adults and pediatrics and optionally infants and neonates in the hospital.
Category
Medical Device
Distribution
29 states
HighFDA (Devices)·Z-1366-2018·2018-04-18
Beckman Coulter iQ200 Urine Analyzer Recall for Barcode Reading Failures
Beckman Coulter is recalling iQ200 Series Urine Microscopy Analyzers because they may fail to read dilution barcodes, causing erroneous results that could delay treatment.
Product
iQ200 Series Urine Microscopy Analyzer with Barcode Reader Model NFT-2100, Catalog #s: 800-3046, 800-3047, 800-3052, 800-3053, 800-3802, 800-3803, 800-3900, 800-3920, 800-3925, 800-3931, 800-3933, 800-3934, 800-3935, 800-3937, 800-3950, 800-3951, 800-3042, 800-3043, 800-3044…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1354-2018·2018-04-18
Bard Premature Infant Feeding Tube Recalled for Ineffective Fusion
C.R. Bard is recalling 42,200 units of Bard Premature Infant Feeding Tubes due to potentially ineffective fusion between the tubing and the ENFit connector.
Product
Bard(R) Premature Infant Feeding Tube, ENFit(TM), REF EN0036400 Product Usage: BARD(R) Nasogastric Sump Tubes with ENFit(TM) connector are intended to be used for: Decompression of stomach by suction or aspiration of gastric contents Short-term administration of term…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0622-2018·2018-04-18
Elroselabs Recalls Molleave OTC Product Due to cGMP Deviations
Elroselabs Inc. is voluntarily recalling Molleave, 2 oz bottles, due to current Good Manufacturing Practice (cGMP) deviations. The product was distributed nationwide.
Product
Molleave, 2 oz bottle, OTC, Manufactured for Elrose Labs, Inc.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1347-2018·2018-04-18
ICU Medical Recalls Infusion Sets with Incorrect Spin Collars
ICU Medical is recalling 7,600 sterile intravascular administration sets because they were manufactured with an incorrect spin collar. The sets were distributed in the US, Canada, and Japan.
Product
14 cm (5.5") Appx 0.27 ml, Smallbore Ext Set w/SURPLUG¿ Nano T-Connector, Clamp, Rotating Luer, 50 pouches per case, Item IR-NG31481B, Sterile, Rx. The firm name on the label is icumedical, San Clemente, CA. The Intravascular Administration Set is a single use, sterile…
Category
Medical Device
Distribution
Distributed nationwide