State

Washington product recalls

73,598 recalls have nationwide distribution and so reach Washington. 8,466 additional recalls listed Washington specifically in their distribution scope.

What the numbers show

Total: 8,466
Critical: 865
Severe: 2,399
Most recent: 2026-10-21

Of the 8,466 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 2,399 (28%) are Severe.

Which agencies issued them

These figures cover only the 8,466 recalls whose distribution notice names Washington specifically. The 73,598 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

28451–28475 of 82064

ModerateFDA (Devices)·Z-1107-2021·2021-02-17
Phadia Recalls EliA dsDNA Well Kits Due to Potential False Positive Results
Phadia US Inc is recalling EliA dsDNA Well kits because decreased positive control values may cause false positive test results for systemic lupus erythematosus.
Product
EliA dsDNA Well - Product Usage: intended for the In-Vitro quantitative measurement of IgG antibodies directed to dsDNA in human serum and plasma as an aid in the clinical diagnosis of systemic lupus erythematosus (SLE). Material Number: 14-5500-01
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0956-2021·2021-02-17
ICU Medical Recalls Smallbore Intravascular Administration Sets Due to Filter Assembly Error
ICU Medical is recalling 7,500 smallbore intravascular administration sets because of an incorrect filter assembly. The affected lots were distributed nationwide and in Belgium.
Product
60" (152 cm) Appx 1.9 ml, Smallbore Ext Set w/MicroClave¿ Clear, 1.2 Micron Filter, 2 Clamps, Luer Lock REF MC330174 - Product Usage: The intravascular administration set is a single use, sterile, non pyrogenic device, which provides access for the administration of fluids from…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1095-2021·2021-02-17
Cardinal Health Recalls Kendall Blue Isolation Gowns Due to Defects
Cardinal Health is recalling Kendall Blue Isolation Gowns due to potential rips, holes, or foreign material that may compromise barrier protection.
Product
Gown Kendall Blue RG, SKU CT5000 Cardinal Health Isolation Gown, Lab Coat, and Kendall" Gowns are intended to provide minimal barrier protection to protect health care patients and health care personnel from the transfer of microorganisms, body fluids and particulate material…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1083-2021·2021-02-17
Cardinal Health Recalls ChemoPlus Chemo Prep and Admin Kits
Cardinal Health is recalling ChemoPlus Chemo Prep & Admin Kits because the included gowns may have defects like rips, holes, or foreign material.
Product
ChemoPlus" Chemo Prep & Admin Kit, CT4025
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1081-2021·2021-02-17
Cardinal Health Recalls ChemoPlus Drug Spill Kits Due to Gown Defects
Cardinal Health is recalling ChemoPlus Drug Spill Kits because the included gowns may have rips, holes, or foreign material.
Product
ChemoPlus Drug Spill Kit-INSTI, SKU DP5016K
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1091-2021·2021-02-17
Cardinal Health Recalls Lab Coats and Gowns Due to Manufacturing Defects
Cardinal Health is recalling approximately 29.8 million lab coats and isolation gowns due to potential manufacturing defects such as rips, holes, and foreign material.
Product
Lab Coats SMS 2X-Large Blue, SKU 2204LC Cardinal Health Isolation Gown, Lab Coat, and Kendall" Gowns are intended to provide minimal barrier protection to protect health care patients and health care personnel from the transfer of microorganisms, body fluids and particulate…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1082-2021·2021-02-17
Cardinal Health Recalls Kendall Spill Kits Due to Gown Defects
Cardinal Health is recalling Kendall Spill Kits because the included gowns may have rips, holes, or foreign material.
Product
Kendall Spill Kit, 6 Per Case, NonsterileI, BB6016K
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1094-2021·2021-02-17
Cardinal Health Recalls Lab Coats and Gowns Due to Defects
Cardinal Health is recalling approximately 29.8 million lab coats and isolation gowns due to potential defects like rips, holes, and foreign material.
Product
Lab Coats SMS 2X-Large White, SKU 2304LC Cardinal Health Isolation Gown, Lab Coat, and Kendall" Gowns are intended to provide minimal barrier protection to protect health care patients and health care personnel from the transfer of microorganisms, body fluids and particulate…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1089-2021·2021-02-17
Cardinal Health Recalls Lab Coats and Gowns Due to Manufacturing Defects
Cardinal Health is recalling approximately 29.8 million lab coats and isolation gowns due to potential rips, holes, and foreign material that may compromise barrier protection.
Product
Lab Coats SMS Large Blue, SKU 2202LC Cardinal Health Isolation Gown, Lab Coat, and Kendall" Gowns are intended to provide minimal barrier protection to protect health care patients and health care personnel from the transfer of microorganisms, body fluids and particulate…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1080-2021·2021-02-17
Cardinal Health Recalls ChemoPlus Drug Spill Kits Due to Gown Defects
Cardinal Health is recalling ChemoPlus Drug Spill Kits because the included gowns may have rips, holes, or foreign material.
Product
CHEMOPLUS DRUG SPILL KIT HOS, SKU CT4004
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1086-2021·2021-02-17
Cardinal Health Recalls Isolation Gowns Due to Potential Rips and Holes
Cardinal Health is recalling isolation gowns and lab coats because they may have rips, holes, or open seams that compromise barrier protection.
Product
Gown Isolation W/Ties Xl Ylw, SKU 1101PG Cardinal Health Isolation Gown, Lab Coat, and Kendall" Gowns are intended to provide minimal barrier protection to protect health care patients and health care personnel from the transfer of microorganisms, body fluids and particulate…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1078-2021·2021-02-17
Cardinal Health Recalls Chemo Spill Kits Due to Gown Defects
Cardinal Health is recalling 137,346 ChemoPlus Chemo Spill Kits because the included gowns may have rips, holes, or foreign material.
Product
Covidien ChemoPlus Chemo Spill Kit, Nonsterile, SKU DP5108K
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0957-2021·2021-02-17
ICU Medical Recalls MicroCLAVE Intravascular Administration Sets Due to Filter Assembly Error
ICU Medical is recalling 7,500 MicroCLAVE intravascular administration sets due to incorrect filter assembly. The affected lots were distributed nationwide in the U.S. and in Belgium.
Product
7 IN (18cm) APPX 0.43ml, SMALLBORE SET, MicroCLAVE, FILTER SetSource - Product Usage: The intravascular administration set is a single use, sterile, non pyrogenic device, which provides access for the administration of fluids from a container to a patient s vascular system…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1106-2021·2021-02-17
Arrow AGB+ Multi-Lumen CVC Kit Recalled for Labeling Error
Arrow International Inc. is recalling 1,705 kits due to a potential product code mislabeling that could cause delays or allergic reactions in sensitive patients.
Product
Arrow AGB+ Multi-Lumen CVC Kit 7Fr 3 Lumen- Intended for venous access to the central circulation by the way of the femoral, jugular, or subclavian veins. Product Code: CDC-45703-1A
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1099-2021·2021-02-17
Cytocell Recalls Aquarius CRLF2 Distal Probe Due to Faint Signal Risk
Cytocell Ltd. is recalling 72 units of the Aquarius LPH 511-A CRLF2 Distal Probe Green because faint additional signals may cause normal samples to be misreported as abnormal.
Product
Aquarius LPH 511-A CRLF2 Distal Probe Green, model no. LPH 511-A The CRLF2 Distal probe, labelled in green, consists of two probes (71kb and 131kb) that are situated distal (telomeric) to the CRLF2 gene
Category
Medical Device
Distribution
7 states
ModerateFDA (Devices)·Z-1097-2021·2021-02-17
Cardinal Health Recalls Kendall Blue XXL Gowns Due to Defects
Cardinal Health is recalling Kendall Blue XXL gowns due to potential rips, holes, or foreign material that may compromise barrier protection.
Product
Gown Kendall Blue XXL, SKU CT5102 Cardinal Health Isolation Gown, Lab Coat, and Kendall" Gowns are intended to provide minimal barrier protection to protect health care patients and health care personnel from the transfer of microorganisms, body fluids and particulate…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1087-2021·2021-02-17
Cardinal Health Recalls Isolation Gowns Due to Potential Rips and Holes
Cardinal Health is recalling isolation gowns and lab coats due to potential defects like rips, holes, and open seams that may compromise barrier protection.
Product
Gown Isolation W/Ties Univ Blu, SKU 1200PG, 2200PG, 552200PG Cardinal Health Isolation Gown, Lab Coat, and Kendall" Gowns are intended to provide minimal barrier protection to protect health care patients and health care personnel from the transfer of microorganisms, body…
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-1092-2021·2021-02-17
Cardinal Health Recalls Lab Coats and Gowns Due to Defects
Cardinal Health is recalling approximately 29.8 million lab coats and gowns due to potential rips, holes, and foreign material that may compromise barrier protection.
Product
Lab Coats SMS Medium White, SKU 2301LC Cardinal Health Isolation Gown, Lab Coat, and Kendall" Gowns are intended to provide minimal barrier protection to protect health care patients and health care personnel from the transfer of microorganisms, body fluids and particulate…
Category
Medical Device
Distribution
Distributed nationwide
LowFDA (Drugs)·D-0250-2021·2021-02-17
Accord Recalls Glycopyrrolate Injection Due to Labeling Mix-up
Accord Healthcare is recalling 502 cartons of Glycopyrrolate Injection due to a packaging error where 2 mL vials were placed in 1 mL blister strips.
Product
GLYCOPYRROLATE — GLYCOPYRROLATE (GLYCOPYRROLATE)
Category
Drug
Distribution
Distributed nationwide
LowFDA (Drugs)·D-0251-2021·2021-02-17
Sun Pharmaceutical Recalls Pantoprazole Sodium Injection Due to Impurity Failures
Sun Pharmaceutical Industries is recalling 20,475 vials of Pantoprazole Sodium for Injection because the product failed impurity and degradation specifications.
Product
PANTOPRAZOLE SODIUM — PANTOPRAZOLE SODIUM (PANTOPRAZOLE SODIUM)
Category
Drug
Distribution
Distributed nationwide
SevereNHTSA·21E012000·2021-02-16
Reyco Granning Recalls Fire Truck Independent Front Suspensions
Reyco Granning is recalling fire truck independent front suspensions because steering gear mounting bolts may loosen, potentially causing steering difficulties or loss of control.
Product
STEERING:CRITICAL FASTENERS recall
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·21E013000·2021-02-16
Ford Recalls Air Bag Inflator Parts for Collision Repair
Ford is recalling specific air bag inflator and module replacement parts used in collision repairs. These parts may explode due to propellant degradation, posing a risk of serious injury or death.
Product
MERCURY — MERCURY, FORD, LINCOLN MILAN, FUSION, MKZ, MUSTANG
Category
Vehicle
Distribution
Distributed nationwide
SevereNHTSA·21V081000·2021-02-16
Ford Recalls Vehicles Due to Air Bag Inflator Explosion Risk
Ford is recalling specific 2004-2014 models because replacement air bag inflators may explode during deployment, potentially causing serious injury or death.
Product
FORD — FORD, MERCURY, LINCOLN FUSION, GT, MILAN, MUSTANG
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·21V074000·2021-02-16
2021 Ford Bronco Sport recall: defective front lower control arms
Ford is recalling certain 2021 Bronco Sport vehicles with defective front lower control arms that may affect handling and increase rollover risk. Owners should contact Ford for a free inspection and replacement.
Product
FORD — FORD BRONCO SPORT
Category
Vehicle
Distribution
Distributed nationwide
HighNHTSA·21V075000·2021-02-16
2021 Ford Bronco Sport recalled for loose rear suspension bolts
Ford is recalling certain 2021 Bronco Sport vehicles because the rear suspension subframe bolts may be loose or missing. Loose bolts could affect vehicle handling and control, increasing the risk of a crash.
Product
FORD — FORD BRONCO SPORT
Category
Vehicle
Distribution
Distributed nationwide