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. 2,612 recalls have been distributed to Washington in the last 12 months.

51,768 total recalls
2,612 in last 12 months

Showing 3052130540 of 51,768 recalls

DrugMay 30, 2017· Mckesson Packaging Services

Recalled Item: BuPROPion HCL Tablets Recalled by Mckesson Packaging Services Due to Failed...

The Issue: Failed Moisture Limits: Product tested out-of-specification for moisture...

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

Class III — Low RiskOngoing
Refund
Medical DeviceMay 30, 2017· ICU Medical, Inc.

Recalled Item: 18 cm (7") PUR Smallbore Ext Set w/6-Port NanoClave¿ Manifold Recalled by...

The Issue: The connection between the Female Luer and the NanoClave¿ manifold has the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 30, 2017· ICU Medical, Inc.

Recalled Item: 10" Smallbore Ext Set w/6-Port NanoClave¿ Manifold (Orange Recalled by ICU...

The Issue: The connection between the Female Luer and the NanoClave¿ manifold has the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 30, 2017· ICU Medical, Inc.

Recalled Item: 10" Smallbore Ext Set w/6-Port NanoClave¿ Manifold Recalled by ICU Medical,...

The Issue: The connection between the Female Luer and the NanoClave¿ manifold has the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 30, 2017· ICU Medical, Inc.

Recalled Item: 168 cm (66") Appx 2.6 ml Recalled by ICU Medical, Inc. Due to The connection...

The Issue: The connection between the Female Luer and the NanoClave¿ manifold has the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 30, 2017· ICU Medical, Inc.

Recalled Item: 28 cm (11") PUR Bifuse Ext Set w/6-Port NanoClave¿ Manifold Recalled by ICU...

The Issue: The connection between the Female Luer and the NanoClave¿ manifold has the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 30, 2017· ICU Medical, Inc.

Recalled Item: 28 cm (11") PUR Smallbore Ext Set w/6-Port NanoClave¿ Manifold Recalled by...

The Issue: The connection between the Female Luer and the NanoClave¿ manifold has the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 30, 2017· ICU Medical, Inc.

Recalled Item: 10" Smallbore Ext Set w/6-Port NanoClave¿ Manifold (Orange Recalled by ICU...

The Issue: The connection between the Female Luer and the NanoClave¿ manifold has the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 30, 2017· ICU Medical, Inc.

Recalled Item: PROXIMALE - 28 cm (11") Smallbore Ext Set w/6-Port NanoClave¿ Manifold...

The Issue: The connection between the Female Luer and the NanoClave¿ manifold has the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 30, 2017· ICU Medical, Inc.

Recalled Item: Kit w/3 Ext Sets Recalled by ICU Medical, Inc. Due to The connection between...

The Issue: The connection between the Female Luer and the NanoClave¿ manifold has the...

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

Class II — Potential Health HazardOngoing
DrugMay 26, 2017· American Pharmaceutical Ingredients LLC

Recalled Item: Methocarbamol Recalled by American Pharmaceutical Ingredients LLC Due to...

The Issue: CGMP Deviations: Lack of quality assurance at the API manufacturer.

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

Class II — Potential Health HazardOngoing
Refund
FoodMay 26, 2017· Smucker Foods of Canada Co.

Recalled Item: Golden Temple No. 1 Fine Durum Atta Flour Blend NET Recalled by Smucker...

The Issue: The firm was notified by their Co-packer that the product may be...

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

Class I — Serious Health HazardOngoing
Refund
FoodMay 26, 2017· Smucker Foods of Canada Co.

Recalled Item: Flour sold under the following brands: Golden Temple Durum Atta Flour Blend...

The Issue: The firm was notified by their Co-packer that the product may be...

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

Class I — Serious Health HazardOngoing
Refund
FoodMay 26, 2017· Monfitello

Recalled Item: Private Selection Peruvian Inspired Aji Amarillo Culinary Spice Paste NET...

The Issue: The firm was notified that the product may contain peanuts.

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

Class I — Serious Health HazardOngoing
Refund
FoodMay 26, 2017· Monfitello

Recalled Item: PRIVATE SELECTION AFRICAN - INSPIRED PERI PERI CHILI CULINARY SPICE Recalled...

The Issue: The firm was notified that the product may contain peanuts.

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

Class I — Serious Health HazardOngoing
Refund
DrugMay 25, 2017· AstraZeneca Pharmaceuticals, LP

Recalled Item: BRILINTA (ticagrelor) tablets Recalled by AstraZeneca Pharmaceuticals, LP...

The Issue: Presence of Foriegn Tablets/Capsules: customer complaint that an 8-count...

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

Class I — Serious Health HazardOngoing
Refund
FoodMay 25, 2017· California Sun Dry Foods

Recalled Item: California Sun Dry Sun Dried Tomato Pesto Recalled by California Sun Dry...

The Issue: Firm employee noticed that incorrect back label was attached to Sun-Dried...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceMay 25, 2017· Becton Dickinson & Company

Recalled Item: BD Insulin Syringes with the BD Ultra-Fine(TM) needle ¿ mL 12.7mm 30G...

The Issue: Product mislabel. Lot 6291768 of the BD Insulin Syringes with the BD...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 25, 2017· Alcon Research, Ltd.

Recalled Item: LX3 Floor Stand for LuxOR Ophthalmic Microscope Recalled by Alcon Research,...

The Issue: Multiple shipments or forceful impact to a caster on a LuxOr/LX3 microscope...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 25, 2017· Atrium Medical Corporation

Recalled Item: Atrium iCAST Balloon Expandable Covered Stent Recalled by Atrium Medical...

The Issue: Firm received a complaint that a customer who ordered an ADVANTA V12 7mm x...

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

Class II — Potential Health HazardOngoing