Product Recalls in Washington

Product recalls affecting Washington — including food, drugs, consumer products, medical devices, and vehicles distributed to Washington. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,765 recalls have been distributed to Washington in the last 12 months.

51,768 total recalls
2,765 in last 12 months

Showing 1480114820 of 51,768 recalls

Medical DeviceNovember 1, 2021· Human Care USA, Inc.

Recalled Item: Hanger-Bar 2P 45cm Recalled by Human Care USA, Inc. Due to The Hanger-Bar is...

The Issue: The Hanger-Bar is being recalled due to the potential for the set screw...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 1, 2021· Smith & Nephew, Inc.

Recalled Item: smith&Nephew EVOS MEDIAL DISTAL FEMUR PLATE Recalled by Smith & Nephew, Inc....

The Issue: Testing vendor notified Smith & Nephew that previous MRI scanning conditions...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 1, 2021· Smith & Nephew, Inc.

Recalled Item: smith&nephew EVOS CONDYLAR MEDIAL DISTAL FEMUR PLATE Recalled by Smith &...

The Issue: Testing vendor notified Smith & Nephew that previous MRI scanning conditions...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 1, 2021· Smith & Nephew, Inc.

Recalled Item: smith&nephew EVOS CONDYLAR MEDIAL DISTAL FEMUR PLATE Recalled by Smith &...

The Issue: Testing vendor notified Smith & Nephew that previous MRI scanning conditions...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 1, 2021· Smith & Nephew, Inc.

Recalled Item: smith&nephew EVOS MEDIAL DISTAL FEMUR PLATE Recalled by Smith & Nephew, Inc....

The Issue: Testing vendor notified Smith & Nephew that previous MRI scanning conditions...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 1, 2021· Randox Laboratories Ltd.

Recalled Item: RANDOX CHOL-cholesterol (total) test system intended to measure cholesterol...

The Issue: When calibrating using the standard provided in the kit, the change in...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
FoodOctober 29, 2021· Mi Piace LLC

Recalled Item: Renata Plant-Based Suprema Pizza Recalled by Mi Piace LLC Due to Undeclared Soy

The Issue: Undeclared soy allergen in frozen pizza

Recommended Action: Do not consume. Return to store for a refund or discard.

Class III — Low RiskOngoing
Refund
FoodOctober 29, 2021· Ingredion Incorporated

Recalled Item: Ingredion INSTANT PURE-FLO F (50 pound bag) food grade starch Recalled by...

The Issue: Potential for metal fragments in product

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceOctober 29, 2021· Diversatek Healthcare

Recalled Item: Diversatek Health Recalled by Diversatek Healthcare Due to M-Catch Retrieval...

The Issue: M-Catch Retrieval Nets, Part Number 1175-01 / Lot Number 001919, that were...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 29, 2021· Philips North America Llc

Recalled Item: Wireless Footswtich used with the following Philips Allura Xper and Recalled...

The Issue: Wireless foot switch connection issues causing interruption of Fluoroscopy...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 29, 2021· NuVasive Specialized Orthopedics, Inc.

Recalled Item: NUVASIVE PRECICE Intramedullary Limb Lengthening (IMLL) and (Short) System:...

The Issue: The Instructions for Use have been updated to include: (1) Clarification...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
DrugOctober 28, 2021· Teva Pharmaceuticals USA

Recalled Item: Clonidine Transdermal System Recalled by Teva Pharmaceuticals USA Due to...

The Issue: Failed Impurities/Degradation Specifications

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
FoodOctober 28, 2021· MARY RUTH ORGANICS

Recalled Item: MaryRuth's Organic Infants Liquid Probiotic Recalled by MARY RUTH ORGANICS...

The Issue: Internal testing found the presence of Pseudomonas aeruginosa in the product.

Recommended Action: Do not consume. Return to store for a refund or discard.

Class I — Serious Health HazardOngoing
Refund
Medical DeviceOctober 28, 2021· Palodex Group Oy

Recalled Item: Orthopantomograph OP300 dental computed tomography x-ray system. The X-ray...

The Issue: It was noticed in production on 28.10.2021, that the final testing database...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 28, 2021· Osteomed, LLC

Recalled Item: OsteoMed OsteoPower Power Console: -OsteoMed OsteoPower Power Console 2 by...

The Issue: Due to consoles not in compliance with the latest electrical safety...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
DrugOctober 27, 2021· Teva Pharmaceuticals USA

Recalled Item: Cartia XT (Diltiazem Hydrochloride Extended-Release Capsules Recalled by...

The Issue: Labelling: Incorrect Exp. Date

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceOctober 27, 2021· Medline Industries Inc

Recalled Item: EVLP Convenience Pack/Kit Recalled by Medline Industries Inc Due to NaCl 250...

The Issue: NaCl 250 mL Bag Inj expired 04/2020 while the kit expiration date was after...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 27, 2021· Medline Industries Inc

Recalled Item: Venous Access Pack-LF Convenience Kit Recalled by Medline Industries Inc Due...

The Issue: NaCl 250 mL Bag Inj expired 04/2020 while the kit expiration date was after...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 27, 2021· Medline Industries Inc

Recalled Item: Major Vascular CDS Convenience Kit Recalled by Medline Industries Inc Due to...

The Issue: NaCl 250 mL Bag Inj expired 04/2020 while the kit expiration date was after...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceOctober 27, 2021· Medline Industries Inc

Recalled Item: Bedside PICC CDS Convenience Kit Recalled by Medline Industries Inc Due to...

The Issue: NaCl 250 mL Bag Inj expired 04/2020 while the kit expiration date was after...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing