State

Washington product recalls

20,096 recalls have nationwide distribution and so reach Washington. 0 additional recalls listed Washington specifically in their distribution scope.

About recalls in Washington

Most US product recalls have nationwide distribution — the manufacturer ships into every state and the recall sweeps the same way. We include those in this listing because they affect Washington consumers even though the source notice doesn’t name the state. State-specific recalls are usually for products with regional distribution (a regional dairy, a local store brand) or where the agency was able to narrow the affected shipments to specific destinations.

If you’re checking whether a recall affects your purchase, the recall detail page lists the exact production lot codes, UPCs, and best-by dates. Match those against your package — distribution scope is a starting filter, not the final answer.

6251–6275 of 20096

HighFDA (Devices)·Z-1002-2025·2025-01-29
Olympus Thunderbeat surgical instrument probe tips may damage or break
Olympus is recalling Thunderbeat surgical hand instruments due to damaged or breaking probe tips that may occur during use and affect surgical procedure safety.
Product
Brand Name: Olympus Thunderbeat Front-Actuated Grip Type S Hand Instrument Product Name: THUNDERBEAT 5 mm,20 cm, Front-actuated Grip Type S Model Number: TB-0520FCS Catalog Number/Product Code: N5424110¿ Software Version: N/A Product Description: Thunderbeat instrument is a
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1011-2025·2025-01-29
Baxter Continu-Flo Solution Set with Duo-Vent Spike recalled for inverted clamps
Baxter is recalling specific lots of Continu-Flo Solution Sets due to potentially inverted side clamps that render the tubing unusable. Distribution included eight US states.
Product
Baxter Continu-Flo Solution Set with Duo-Vent Spike, REF UC8519
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0998-2025·2025-01-29
Olympus Thunderbeat Surgical Instrument Recalled for Damaged or Breaking Probe Tips
Olympus is recalling approximately 9,200 units of Thunderbeat surgical hand instruments distributed worldwide because probe tips can become damaged, break, or pads can detach during use.
Product
Brand Name: Olympus Thunderbeat Front-Actuated Grip Type S Hand Instrument Product Name: THUNDERBEAT 5 mm,45 cm,Front-actuated Grip Type S Model Number: TB-0545FCS Catalog Number/Product Code: N5423330 Software Version: N/A Product Description: Thunderbeat instrument is a s
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0985-2025·2025-01-29
Medtronic Recalls EOPA Arterial Cannula Models for Labeling Errors
Medtronic Perfusion Systems is recalling EOPA Arterial Cannula models 77418 and 77422 due to incorrect labeling on seven manufacturing lots. Approximately 930 units were distributed worldwide.
Product
EOPA Arterial Cannula, Model Numbers 77422 (22 Fr) and 77418 (18 Fr)
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1005-2025·2025-01-29
Medical Analyzer Software May Fail to Alert of Expired Reagent Packs
The VITROS 5600 Integrated System's software (version 3.8.0 and higher) may fail to notify users when Signal Reagent Packs expire. This could result in use of expired reagents, causing no results or erroneous results from tests.
Product
Brand Name: VITROS Product Name: VITROS 5600 Integrated System Model/Catalog Number: 6802413 (New), 6802415 (Certified/Refurbished), 6904001 (China) Software Version: version 3.8.0 or higher Product Description: In vitro diagnostic chemistry analyzer. FDA 3 letter product
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0963-2025·2025-01-29
Otological Ventilation Tubes Recalled for Missing FDA 510(k) Clearance
Adept Medical Ltd is recalling 13,070 Otological Ventilation Tubes because they were distributed without FDA 510(k) clearance. Over 9,000 units were distributed in the US and 3,980 internationally.
Product
Otological Ventilation Tube - T-Tube 6mm - Silicone; Product Code: NZ3306/NZ3306-2;
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1009-2025·2025-01-29
Baxter Solution Set with Duo-Vent Spike Recalled for Inverted Clamps
Baxter Healthcare is recalling specific lots of its Solution Set with Duo-Vent Spike due to inverted side clamps that may render the tubing unusable. The affected product was distributed nationwide.
Product
Baxter Solution Set with Duo-Vent Spike, REF 2R8404
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0983-2025·2025-01-29
HALYARD Laparotomy Surgical Pack Recalled for Additive Residue Contamination
O&M HALYARD is recalling HALYARD Laparotomy Packs due to elevated residues of anti-block/slip additives found in the sterile packaging. These surgical instruments were distributed nationwide.
Product
Brand Name: HALYARD Product Name: Laparotomy Pack Model/Catalog Number: 88231 Software Version: N/A Product Description: Laparotomy Pack Component: N/A
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0981-2025·2025-01-29
Stryker neurosurgical device labeling mismatch: wrong instruments shipped
Stryker is recalling 3.0MM Neuro Match Head devices (REF 5820-107-430) where the actual device may not match the product label, potentially causing surgeons to use wrong instruments during neurosurgery.
Product
stryker 3.0MM Neuro Match Head, REF 5820-107-430, used to cut bone and bone cement during neurosurgery
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1012-2025·2025-01-29
Dressing change kits recalled due to packaging defect compromising sterility
Trinity Sterile is recalling Dressing Change Kits with ChloraPrep and HaloGUARD due to potential holes in the package that could compromise product sterility. The recall affects 1,980 units distributed across multiple states.
Product
Brand Name: IMed Products Product Name: Dressing Change Kit with ChloraPrep 3mL & HaloGUARD Model/Catalog Number: IM46062 Software Version: N/A Product Description: Dressing change kit, case of 30, lot #600022, 66 cases affected. Component: No
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-0993-2025·2025-01-29
Olympus Thunderbeat surgical instrument probe tips breaking and detaching
Olympus is recalling Thunderbeat surgical instruments due to probe tip damage, breaking, and pad detachment.
Product
Brand Name: Olympus Thunderbeat Front-Actuated Grip Type S Hand Instrument Product Name: THUNDERBEAT 5 mm, 35 cm, Front-actuated Grip Type S Model Number: TB-0535FCS Catalog Number/Product Code: R5000687 Software Version: N/A Product Description: Thunderbeat instrument is a
Category
Medical Device
Distribution
Distributed nationwide
HighFDA (Devices)·Z-1014-2025·2025-01-29
Dressing Change Kits Recalled for Potential Package Sterility Compromise
Trinity Sterile is recalling Wolf-Pak Dressing Change Kits due to a potential hole in the package that could compromise the sterility of the medical kit. Lot #600022 (3,960 units) distributed nationwide.
Product
Brand Name: Wolf-Pak Product Name: Dressing Change Kit with Cloth Border Tegaderm Dressing & 3mL CHG One Step Applicator CS/30 Model/Catalog Number: DC3080LF Software Version: N/A Product Description: Dressing change kit, case of 30, lot #600022, 132 cases affected. Componen
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0205-2025·2025-01-29
Kissable Diabetics Foot Cream recalled nationwide for inadequate release testing
Brands International Corporation is recalling Kissable Diabetics Foot Cream nationwide due to lack of adequate release testing during manufacturing. The FDA has classified this as a Class II recall.
Product
Kissable Diabetics Foot Cream, NET WT 4 oz (113 g) per tube, Manufactured By: Brands International Corp., Newmarket, ON, L3X 2S2. UPC 6 72008 80925 3
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0977-2025·2025-01-29
Programmable Valve Device Recalled Due to Incorrect Product Description Labels
CODMAN CERTAS Plus Programmable Valve (Model 828810) units were distributed with incorrect product descriptions on labels. 132 units affected across multiple U.S. states and international locations.
Product
CODMAN CERTAS Plus Programmable Valve Inline Small Valve Only. Model Number: 828810 Implantable device that provides constant intraventricular pressure and drainage of CSF for the management of hydrocephalus.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0980-2025·2025-01-29
Stryker Surgical Burs Recalled Due to Package Label Mismatch
Stryker Corporation is recalling surgical burs that may be packaged with incorrect labels, causing a mismatch between the device model inside and the label. Approximately 491 affected devices were distributed worldwide.
Product
The 3.0MM Neuro Match Head Soft Touch bur (5820-107-030) is intended to be used to cut bone and bone cement during neurosurgery, including craniotomy and spinal surgery as well as ear, nose and throat (ENT)/Otology/Neurotology/ Otorhinolaryngology, orthopedic, and general surgic
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0984-2025·2025-01-29
Medtronic Pediatric Arterial Cannulae Recalled for Incorrect Labeling
Medtronic is recalling 745 DLP Pediatric Arterial Cannulae (Models 77008 and 77014) due to incorrect labeling affecting seven manufactured lots distributed nationwide and worldwide.
Product
DLP Pediatric One-Piece Arterial Cannulae, Model Numbers 77008 (8 Fr) and 77014 (14 Fr)
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Drugs)·D-0208-2025·2025-01-29
Venlafaxine Extended-Release Tablets Recalled for Missing Tablet Identification
Appco Pharma LLC is recalling Venlafaxine Extended-Release Tablets, 150mg, due to missing tablet identification imprints. The defect affects 1,380 bottles distributed nationwide.
Product
VENLAFAXINE — VENLAFAXINE (VENLAFAXINE)
Category
Drug
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0979-2025·2025-01-29
CODMAN CERTAS Plus programmable valve recalled for incorrect label descriptions
Integra LifeSciences is recalling 46 units of the CODMAN CERTAS Plus Programmable Valve due to incorrect product descriptions on internal and external labels. The affected devices were distributed nationwide across the U.S. and internationally.
Product
CODMAN CERTAS Plus Programmable Valve Right Angle Valve Only. Model Number: 828820. Implantable device that provides constant intraventricular pressure and drainage of CSF for the management of hydrocephalus.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0986-2025·2025-01-29
Medtronic Arterial Cannula Recall Due to Incorrect Labeling
Medtronic Perfusion Systems is recalling Select Series Angled Tip Arterial Cannulas (Model 72422) due to incorrect labeling. The recall involves 440 units distributed nationwide.
Product
Select Series Angled Tip Arterial Cannula, Model Number 72422 (22 Fr)
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0969-2025·2025-01-29
Otological Ventilation Tubes Recalled for Lack of FDA 510(k) Clearance
Adept Medical Ltd is recalling 2,440 otological ventilation tubes due to lack of FDA 510(k) regulatory clearance. The recall affects 1,940 units in the US and 500 units distributed internationally.
Product
Otological Ventilation Tube - Donaldson - Blue Silicone; Product Code: NZ3321;
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0964-2025·2025-01-29
Otological Ventilation Tubes Distributed Without FDA 510(k) Clearance
Adept Medical Ltd is recalling 2,010 units of T-Tube 6mm Double Silicone otological ventilation tubes distributed without required FDA 510(k) clearance. The recall affects 630 US units and 1,380 international units.
Product
Otological Ventilation Tube - T-Tube 6mm - Double - Silicone; Product Code: NZ3306-2;
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0978-2025·2025-01-29
Integra implantable hydrocephalus valve recalled for incorrect product description on labels
Integra LifeSciences is recalling CODMAN CERTAS Plus Programmable Valves (Model 828810PL) due to incorrect product descriptions on internal and external labels. The mislabeling affects 170 units distributed across the US and several international locations.
Product
CODMAN CERTAS Plus Programmable Valve Inline Small Valve Only. Model Number: 828810PL. Implantable device that provides constant intraventricular pressure and drainage of CSF for the management of hydrocephalus.
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0967-2025·2025-01-29
Otological Ventilation Tube Recalled Due to Lack of Regulatory Clearance
Adept Medical Ltd is recalling otological ventilation tubes distributed without FDA 510(k) clearance. The recall affects approximately 2,190 units in the US.
Product
Otological Ventilation Tube - T-Tube 12mm - Silicone; Product Code: NZ3312;
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0970-2025·2025-01-29
Otological Ventilation Tube Recalled Due to Lack of FDA Clearance
Adept Medical Ltd is recalling otological ventilation tubes distributed without FDA 510(k) clearance. The recall affects 4,080 units distributed in the US and internationally.
Product
Otological Ventilation Tube - Donaldson - Double - Blue Silicone; Product Code: NZ3321-2;
Category
Medical Device
Distribution
Distributed nationwide
ModerateFDA (Devices)·Z-0968-2025·2025-01-29
Otological Ventilation Tubes recalled due to lack of FDA 510(k) clearance
Adept Medical Ltd is recalling 310 units of Otological Ventilation Tubes (Product Code NZ3312-2) distributed in the US and internationally due to lack of FDA 510(k) regulatory clearance. The devices were distributed without required FDA pre-market approval.
Product
Otological Ventilation Tube - T-Tube 12mm - Double - Silicone; Product Code: NZ3312-2;
Category
Medical Device
Distribution
Distributed nationwide