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. 2,789 recalls have been distributed to Washington in the last 12 months.

51,768 total recalls
2,789 in last 12 months

Showing 1250112520 of 51,768 recalls

Medical DeviceJune 2, 2022· CHANGZHOU BIOMET MEDICAL DEVICES CO., LTD.

Recalled Item: DVR Anatomic Recalled by CHANGZHOU BIOMET MEDICAL DEVICES CO., LTD. Due to...

The Issue: One lot of DVRASL plates were incorrectly etched and may have been placed...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 2, 2022· Skytron, Div. The KMW Group, Inc

Recalled Item: Product Name: GCX Channel Mounting Accessory Model/Catalog Number:...

The Issue: Under certain circumstances, the mounting screws may loosen or pull out from...

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

Class II — Potential Health HazardOngoing
FoodJune 1, 2022· Taylor Farms Retail Inc

Recalled Item: Trader Joe's BBQ & Black Pepper Toscano Chopped Salad 11 oz. Contains Milk...

The Issue: Undeclared allergen (peanuts) from incorrect master pack. Salad kit contains...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJune 1, 2022· GE Healthcare, LLC

Recalled Item: GE Healthcare Aisys CS2 Anesthesia System Recalled by GE Healthcare, LLC Due...

The Issue: There is a potential reversal of the O2 and air cylinder pressure transducer...

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

Class I — Serious Health HazardOngoing
Medical DeviceJune 1, 2022· RAYSEARCH LABORATORIES AB

Recalled Item: RayStation 9B SP1. For radiation treatment planning. Recalled by RAYSEARCH...

The Issue: An issue with propagation of treatment course information from RayStation...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 1, 2022· Ventana Medical Systems Inc

Recalled Item: Ventana HE 600 System Recalled by Ventana Medical Systems Inc Due to There...

The Issue: There is a potential for fluid leak inside the Ventana HE 600 instrument...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 1, 2022· Ultradent Products, Inc.

Recalled Item: Peak Universal Bond Self-Etch Bottle Kit Recalled by Ultradent Products,...

The Issue: SE primer may be missing some or all of the resin portion of the chemistry....

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 1, 2022· Fresenius Medical Care Holdings, Inc.

Recalled Item: NaturaLyte 2301 2K 3.0 Ca 1 Mg Gal Recalled by Fresenius Medical Care...

The Issue: The product was potentially exposed to below-recommended storage...

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

Class II — Potential Health HazardOngoing
FoodMay 31, 2022· THISTLE HEALTH INC

Recalled Item: Thistle Tropical Limeade Cold-Pressed Organic Juice watermelon pineapple...

The Issue: Manufactured using organic strawberries potentially contaminated with Hep A.

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

Class II — Potential Health HazardOngoing
Refund
FoodMay 31, 2022· THISTLE HEALTH INC

Recalled Item: Thistle Watermelon Berry Cold-Pressed Organic Juice watermelon strawberry...

The Issue: Manufactured using organic strawberries potentially contaminated with Hep A.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMay 31, 2022· Spacelabs Healthcare, Inc.

Recalled Item: Xhibit Telemetry Receiver Recalled by Spacelabs Healthcare, Inc. Due to...

The Issue: Software related alarm escalation defect occurs after approximately 25 days...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 31, 2022· Baxter Healthcare Corporation

Recalled Item: NaviCare Nurse Call/Voalte Nurse Call Recalled by Baxter Healthcare...

The Issue: An issue has been identified with Phillips (Emergin) and Longleaf non relay...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 30, 2022· Ossur Americas

Recalled Item: OSSUR VARIFLEX SUBA JUNIOR foot and ankle external prosthesis Recalled by...

The Issue: Due to receiving complaints related to broken (cracked) prosthetic foot with...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 27, 2022· Medtronic Neuromodulation

Recalled Item: LEAD 3387S-40 STIMLOC DBS Recalled by Medtronic Neuromodulation Due to There...

The Issue: There are a small number of units of the DBS Lead with StimLoc kit...

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

Class II — Potential Health HazardOngoing
DrugMay 26, 2022· Amazon.com, Inc.

Recalled Item: Artri Ajo King con Ortiga y Omega 3 tablets Recalled by Amazon.com, Inc. Due...

The Issue: Marketed Without An Approved NDA/ANDA: FDA laboratory analysis found the...

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

Class I — Serious Health HazardOngoing
Refund
DrugMay 26, 2022· Amazon.com, Inc.

Recalled Item: Ortiga mas Ajo Rey con Omega 3 Recalled by Amazon.com, Inc. Due to...

The Issue: Marketed Without An Approved NDA/ANDA: FDA laboratory analysis found the...

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

Class I — Serious Health HazardOngoing
Refund
DrugMay 26, 2022· Amazon.com, Inc.

Recalled Item: Artri King con Ortiga y Omega 3 tablets Recalled by Amazon.com, Inc. Due to...

The Issue: Marketed Without An Approved NDA/ANDA: FDA laboratory analysis found the...

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

Class I — Serious Health HazardOngoing
Refund
FoodMay 26, 2022· Albanese Confectionery Group, Inc.

Recalled Item: Rich s Milk Chocolate Giant Layered Peanut Butter and Cups Recalled by...

The Issue: Salmonella. Product made using recalled Jif peanut butter

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceMay 26, 2022· Paragon 28, Inc.

Recalled Item: HammerTube Implant Recalled by Paragon 28, Inc. Due to Due to Titanium...

The Issue: Due to Titanium plasma coating not present implant.

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 26, 2022· Ortho-Clinical Diagnostics, Inc.

Recalled Item: Anti-SARS-CoV-2 IgG Quantitative Reagent Pack- Intended for use on VITROS¿...

The Issue: On-Analyzer Stability (OAS) time, supported for 6 weeks; not 8 weeks as is...

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

Class II — Potential Health HazardOngoing