State

Washington product recalls

73,570 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: 868
Severe: 2,396
Most recent: 2026-10-21

Of the 8,466 recalls naming Washington we have scored against our rubric, 868 (10%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 2,396 (28%) are Severe.

Which agencies issued them

These figures cover only the 8,466 recalls whose distribution notice names Washington specifically. The 73,570 nationwide recalls listed below reach every state, so counting them here would make every state page show the same numbers.

25726–25750 of 82036

HighFDA (Food)·F-1010-2021·2021-09-29
Baker's Corner Oatmeal Cranberry Cookies Recalled for Undeclared Soybean Oil
Baker's Corner Bakery is recalling Oatmeal Cranberry Cookies because soybean oil is not declared on the label, despite being present in the shortening ingredient. Consumers with soy allergies may be at risk.
Product
Oatmeal Cranberry Cookie, packed in closed bags, 12oz net wt. The label of affected product is read in parts: "***Oatmeal Cranberry Cookie*** Ingredients: Oats, dried cranberries, Shepherds Grain Flour (wheat flour, malted barley flour, niacin, reduced iron, thiamine…
Category
Food
Distribution
1 state
HighFDA (Devices)·Z-2527-2021·2021-09-29
C.R. Bard SureStep Foley Catheter Tray Sterile Barrier Defect Recall
C.R. Bard is recalling 5,950 SureStep Foley Tray kits nationwide due to potential packaging defects that may impact the sterile barrier.
Product
Catalog A319416AM, SureStep" Foley Tray, Bardex" I.C., Complete Care", Urine Meter, Temperature Sensing, StatLock" Stabilization Device
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2502-2021·2021-09-29
Centricity PACS Medical Imaging System Image Acquisition and Synchronization Failures
GE Healthcare's Centricity PACS-IW system experiences image acquisition and synchronization failures that could impair the display of medical images. The software malfunction affects 392 devices globally.
Product
Centricity PACS-IW with Universal Viewer - Product Usage: Is a device that displays medical images (including mammograms) and data from various imaging sources.
Category
Medical Device
Distribution
34 states
HighFDA (Devices)·Z-2512-2021·2021-09-29
Univation X Knee Implant Devices Recalled Due to Loosening Risk
Aesculap Implant Systems is recalling Univation X System knee implant devices (all lots, nationwide) because the implants may loosen, potentially requiring revision surgery. No injuries have been reported.
Product
Univation X System knee implant devices as follows: Catalog/Product: NL488 UNIVATION F MENISCAL COMP.T1 RM/LM 10MM; NL489 UNIVATION F MENISCAL COMP.T2 RM/LM 10MM; NL490 UNIVATION F MENISCAL COMP.T3 RM/LM 10MM; NL491 UNIVATION F MENISCAL COMP.T4 RM/LM 10MM; NL492 UNIVATION…
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2507-2021·2021-09-29
Greiner VACUETTE 2 ml Coagulation Blood Collection Tubes Anticoagulant and Vacuum Recall
Greiner Bio-One is recalling 956,400 VACUETTE coagulation blood collection tubes that may clot due to anticoagulant variation or low vacuum.
Product
Greiner Bio-One VACUETTE¿ TUBE 2 ml 9NC Coagulation sodium citrate 3.2% 13x75 blue cap-white ring, sandwich tube, non-ridged
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2529-2021·2021-09-29
Foley Catheter Tray Recalled Due to Potential Packaging Defects
C.R. Bard is recalling 2,660 units of SureStep Foley Catheter Trays nationwide due to potential packaging defects that may impact the sterile barrier.
Product
Catalog A800061, SureStep" Foley Tray, Bard LubricathTM Foley Catheter Tray
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2521-2021·2021-09-29
C.R. Bard SureStep Foley Tray Recalled for Packaging Defect Risk
C.R. Bard is recalling SureStep Foley Tray units due to potential packaging defects that may compromise the sterile barrier. The recalled product was distributed nationwide in the United States.
Product
Catalog A119216M, SureStep" Foley Tray, Lubri-Sil", Urine Meter, Temperature Sensing Dual, StatLock" Stabilization Device
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Drugs)·D-0812-2021·2021-09-29
Metoprolol Tartrate Tablets Recalled for Metal Wire Contamination
Aurobindo Pharma USA Inc. is recalling Metoprolol Tartrate 100 mg tablets due to the presence of metal wire found in at least one tablet. The FDA classified this as a Class II recall affecting 2,820 bottles distributed nationwide.
Product
METOPROLOL TARTRATE — METOPROLOL TARTRATE (METOPROLOL TARTRATE)
Category
Drug
Distribution
Distributed nationwide
HighNHTSA·21V769000·2021-09-29
Class A motorhomes recalled for instrument cluster blanking while in motion
Jayco is recalling certain 2019-2021 Entegra and Jayco Class A motorhomes because the instrument cluster may go blank while driving, potentially hiding speed and warning lights.
Product
JAYCO — JAYCO, ENTEGRA EMBARK, ANTHEM, ASPIRE, CORNERSTONE
Category
Vehicle
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2535-2021·2021-09-29
SureStep Foley Tray Recall: Packaging Defects May Compromise Sterile Barrier
C.R. Bard Inc is recalling SureStep Foley Trays (Catalog A902616) due to packaging defects that may compromise the sterile barrier. Affected units were distributed nationwide.
Product
Catalog A902616, SureStep" Foley Tray, Bardex" I.C., Lubricath", Urine Meter
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2501-2021·2021-09-29
Scorpion Portal Vein Access Set Recalled for Cracking Sheaths
Argon Medical Devices is recalling the Scorpion Portal Vein Access Set due to design changes that have caused the sheaths to crack or break at the tips. The affected product was distributed in the United States.
Product
Scorpion Portal Vein Access Set - Product Usage: used to gain access to the hepatic vein and guide a sharp puncture tool (0.040 Stylet or 17ga Needle) through the parenchyma.
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-2494-2021·2021-09-29
Ad-Tech Medical Cable Recalled Due to Incorrect Product Labels
Ad-Tech Lightweight CABRIO Cables with incorrect labels are being recalled. Mislabeling could cause product misidentification affecting proper use in clinical monitoring applications.
Product
Ad-Tech Lightweight CABRIO Cable - Product Usage: Designed for the purpose of connecting these electrodes to third party monitors/stimulators.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0809-2021·2021-09-29
Pfizer recalls Chantix tablets for N-nitroso-varenicline impurity
Pfizer is recalling certain lots of Chantix (varenicline tartrate) 0.5mg tablets nationwide due to the presence of N-nitroso-varenicline impurity above FDA's acceptable interim intake limit.
Product
CHANTIX — CHANTIX (VARENICLINE TARTRATE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2495-2021·2021-09-29
Ad-Tech TECH ATTACH Cable Recalled for Incorrect Label Information
Ad-Tech Medical recalled its Lightweight TECH ATTACH Cable due to incorrect labels on affected units. The cables are designed to connect electrodes to third-party monitors and stimulators.
Product
Ad-Tech Lightweight TECH ATTACH Cable - Product Usage: Designed for the purpose of connecting these electrodes to third party monitors/stimulators.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0813-2021·2021-09-29
Sirolimus Tablets Recalled for Failed Impurities and Degradation Specifications
American Health Packaging is recalling Sirolimus 1 mg tablets (Lot #1000789, expiring 10/31/2022) distributed nationwide because they failed impurities and degradation specifications.
Product
SIROLIMUS — SIROLIMUS (SIROLIMUS)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0823-2021·2021-09-29
Drug Recall: Chlorzoxazone Tablets Due to Manufacturing Deviations
Glenmark Pharmaceuticals is recalling 1,800 bottles of Chlorzoxazone Tablets USP 375 mg nationwide due to current Good Manufacturing Practice (CGMP) deviations. The recall was initiated on August 27, 2021.
Product
Chlorzoxazone Tablets USP 375 mg 100 Tablets Rx Only NDC 68462-724-01 Manufactured by: Glenmark Pharmaceuticals Inc., USA 4147 Goldmine Road Monroe, NC 28110 Manufactured for: Glenmark Pharmaceuticals Inc., USA Mahwah, NJ 07430
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0828-2021·2021-09-29
Betadine Povidone-Iodine Solution Swabstick recalled for subpotent drug
Avrio Health L.P. is recalling Betadine Solution Swabstick in single and three-count packages nationwide because the product is subpotent—meaning it contains less active ingredient than specified. Consumers should stop using affected lots and consult their healthcare provider if needed.
Product
BETADINE — BETADINE (POVIDONE-IODINE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0808-2021·2021-09-29
Chantix Varenicline Tablets Recalled for Nitroso Impurity
Pfizer is recalling Chantix (varenicline) tablets nationwide due to the presence of N-nitroso-varenicline impurity above FDA's acceptable interim intake limit, a manufacturing deviation.
Product
Chantix (varenicline) tablets 0.5mg/1mg, 56 Tablets, Rx only, Distributed by Pfizer Labs, Division of Pfizer Inc. NY, NY 10017, Made in Ireland, NDC 00069-0471-03. carton containing one blister pack of 11 0.5 mg tablets and one blister pack containing 42.1 mg tablets.
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2496-2021·2021-09-29
Ad-Tech TECH ATTACH Cable Recalled Due to Incorrect Labeling
Ad-Tech Medical Instrument Corporation is recalling TECH ATTACH Cables due to incorrect labeling. The cables connect electrodes to third-party monitors and stimulators.
Product
Ad-Tech TECH ATTACH Cable- Product Usage: Designed for the purpose of connecting these electrodes to third party monitors/stimulators.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0824-2021·2021-09-29
Chlorzoxazone 750 mg Tablets Recalled Due to CGMP Deviations
Glenmark Pharmaceuticals is recalling Chlorzoxazone 750 mg tablets nationwide due to current good manufacturing practice (CGMP) deviations. The voluntary recall affects 4,752 bottles with five affected lot numbers.
Product
Chlorzoxazone Tablets USP 750 mg 100 Tablets Rx Only NDC 68462-725-01 Manufactured by: Glenmark Pharmaceuticals Inc., USA 4147 Goldmine Road Monroe, NC 28110 Manufactured for: Glenmark Pharmaceuticals Inc., USA Mahwah, NJ 07430
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0814-2021·2021-09-29
Promethazine Syrup Plain Recall Due to Microbial Contamination
Morton Grove Pharmaceuticals is recalling Promethazine Syrup Plain 6.25 mg/5 mL in 1-pint bottles due to potential microbial contamination in liquid sugar batches used during manufacturing.
Product
Promethazine Syrup Plain, 6.25 mg/5 mL (Promethazine Hydrochloride Syrup, USP), 1 Pint (473 mL), Rx Only, Manufactured For: Wockhardt USA, LLC, Parsippany, NJ 07054; Manuractured By: Morton Grove Pharmaceuticals, Inc, Morton Grove, IL 60053. NDC: 60432-608-16
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0810-2021·2021-09-29
Chantix Varenicline Tablets Recalled for N-Nitroso Impurity
Pfizer is recalling specific lots of Chantix (varenicline) 1 mg tablets nationwide due to the presence of N-nitroso-varenicline impurity above FDA's acceptable interim intake limit. The affected lots were distributed nationwide.
Product
CHANTIX — CHANTIX (VARENICLINE TARTRATE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0816-2021·2021-09-29
Valproic Acid Oral Solution recalled for microbial contamination
Morton Grove Pharmaceuticals is recalling Valproic Acid Oral Solution (250 mg/5 mL) due to potential microbial contamination in liquid sugar batches used during manufacturing.
Product
Valproic Acid Oral Solution USP, (250 mg/5 mL), 1 Pint (473 mL), Rx Only, Manufactured For: Wockhardt USA, LLC, Parsippany, NJ 07054; Manuractured By: Morton Grove Pharmaceuticals, Inc, Morton Grove, IL 60053. NDC: 60432-621-16
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0825-2021·2021-09-29
Zonisamide Capsules Recalled for Manufacturing Deviations
Glenmark Pharmaceuticals is recalling Zonisamide Capsules 50 mg nationwide due to manufacturing deviations. The recall affects approximately 15,936 bottles across multiple lots with expiration dates in May 2022.
Product
ZONISAMIDE — ZONISAMIDE (ZONISAMIDE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-2486-2021·2021-09-29
Microbiologics SARS-CoV-2 Process Control Pellets Recalled for Product Specification Issue
Microbiologics Inc is recalling 218 units of SARS-CoV-2 process control pellets (catalog HE0062S) used to validate diagnostic tests. The FDA Class II recall involves product composition regarding RNA transcript content.
Product
SARS-CoV-2 Process Control (Pellet) - Product Usage: intended for use as an external, non-viable control material to evaluate the performance of nucleic acid tests that detect SARS-CoV-2 virus.
Category
Medical Device
Distribution
Distributed nationwide