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. 2,653 recalls have been distributed to Washington in the last 12 months.

51,768 total recalls
2,653 in last 12 months

Showing 2386123880 of 51,768 recalls

DrugMarch 22, 2019· InvaGen Pharmaceuticals, Inc.

Recalled Item: Testosterone Cypionate Injection Recalled by InvaGen Pharmaceuticals, Inc....

The Issue: Presence of Particulate Matter.

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 22, 2019· InvaGen Pharmaceuticals, Inc.

Recalled Item: Testosterone Cypionate Injection Recalled by InvaGen Pharmaceuticals, Inc....

The Issue: Presence of Particulate Matter.

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 22, 2019· Auro Pharmacies Inc. DBA Central Drugs

Recalled Item: Biotin 10 mg/mL Injection Recalled by Auro Pharmacies Inc. DBA Central Drugs...

The Issue: Failed pH Specification: product does not meet pH label claim.

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

Class III — Low RiskOngoing
Refund
DrugMarch 22, 2019· Lupin Pharmaceuticals Inc.

Recalled Item: Fayosim (levonorgestrel and ethinyl estradiol) tablets USP Recalled by Lupin...

The Issue: Failed Impurities/Degradation Specifications: Out-of-specification results...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMarch 22, 2019· Stryker Communications

Recalled Item: Berchtold Chromophare F628 Surgical Lights. Product Usage: The medical...

The Issue: The back cover of the light head was insufficiently assembled and could...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 22, 2019· Stryker Communications

Recalled Item: Berchtold Chromophare F528 Surgical Lights. Product Usage: The medical...

The Issue: The back cover of the light head was insufficiently assembled and could...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 22, 2019· Cardinal Health 200, LLC

Recalled Item: ChemoPlus Chemo Spill Kit Product Code:CT4004 Product Usage: ChemoPlus...

The Issue: Kit label states not made with natural rubber latex,however safety goggles...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 22, 2019· Siemens Medical Solutions USA, Inc

Recalled Item: Cios Alpha with software version VA30-mobile C-arm x-ray Material # Recalled...

The Issue: Continuous operation of the Cios Alpha at high tube outputs may result in...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 22, 2019· Cardinal Health 200, LLC

Recalled Item: ChemoPlus Chemo Spill Kit Recalled by Cardinal Health 200, LLC Due to Kit...

The Issue: Kit label states not made with natural rubber latex,however safety goggles...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 22, 2019· Cardinal Health 200, LLC

Recalled Item: ChemoPlus Protective Wrap-around Goggles Product Code:DP5030G Product Usage:...

The Issue: Kit label states not made with natural rubber latex,however safety goggles...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 22, 2019· Cardinal Health 200, LLC

Recalled Item: ChemoPlus Chemo Spill Kit Product Code:DP5016K Product Usage: ChemoPlus...

The Issue: Kit label states not made with natural rubber latex,however safety goggles...

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

Class II — Potential Health HazardOngoing
FoodMarch 21, 2019· Impossible Foods

Recalled Item: Impossible Foods Bulk Recalled by Impossible Foods Due to Piece of plastic...

The Issue: Piece of plastic was found in bulk product.

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

Class II — Potential Health HazardOngoing
Refund
FoodMarch 21, 2019· Allen's Blueberry Freezer, Inc.

Recalled Item: Wild Sweet ALLEN'S BLUEBERRIES WILD BLUEBERRIES IQF 30 LBS. NET Recalled by...

The Issue: Product tested positive for E.coli O157:H7 STEC.

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

Class I — Serious Health HazardOngoing
Refund
FoodMarch 21, 2019· Better Made Snack Foods Inc.

Recalled Item: Better Made Snack Foods Family Size $3.99 Original Potato Chips Recalled by...

The Issue: Undeclared milk

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMarch 21, 2019· Community Products, LLC

Recalled Item: Rifton TRAM Standard Base Recalled by Community Products, LLC Due to A...

The Issue: A design change to the load-bearing quick release buckle renders the springs...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 21, 2019· Community Products, LLC

Recalled Item: Rifton TRAM Low Base Recalled by Community Products, LLC Due to A design...

The Issue: A design change to the load-bearing quick release buckle renders the springs...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 21, 2019· Community Products, LLC

Recalled Item: Rifton E-Pacer Recalled by Community Products, LLC Due to A design change to...

The Issue: A design change to the load-bearing quick release buckle renders the springs...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 21, 2019· Flowonix Medical Inc

Recalled Item: Prometra Programmable Pump Recalled by Flowonix Medical Inc Due to The pump...

The Issue: The pump shuts down unexpectedly if Error 115, an alarm associated with a...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 21, 2019· Flowonix Medical Inc

Recalled Item: Prometra Clinician Programmer (Touchscreen) Software version 2.00.29...

The Issue: The pump shuts down unexpectedly if Error 115, an alarm associated with a...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 21, 2019· Flowonix Medical Inc

Recalled Item: Prometra Programmer (Grand Prime) Software version 2.00.29 Recalled by...

The Issue: The pump shuts down unexpectedly if Error 115, an alarm associated with a...

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

Class II — Potential Health HazardOngoing