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 2922129240 of 51,768 recalls

DrugSeptember 1, 2017· Pharmedium Services, LLC

Recalled Item: Oxytocin 10 units added to 500 mL Lactated Ringer's Injection USP in 500 mL...

The Issue: Subpotent Drug

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 1, 2017· Pharmedium Services, LLC

Recalled Item: Oxytocin 10 units added to 1000 mL Lactated Ringer's Injection Recalled by...

The Issue: Subpotent Drug

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 1, 2017· Pharmedium Services, LLC

Recalled Item: Oxytocin 20 units added to 1000 mL Lactated Ringer's Injection Recalled by...

The Issue: Subpotent Drug

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 1, 2017· Pharmedium Services, LLC

Recalled Item: Oxytocin 30 units added to 500 mL Lactated Ringer's USP in 500 mL bag...

The Issue: Subpotent Drug

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 1, 2017· Pharmedium Services, LLC

Recalled Item: Oxytocin 20 units added to 1000 mL Lactated Ringer's Injection Recalled by...

The Issue: Subpotent Drug

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 1, 2017· Pharmedium Services, LLC

Recalled Item: Oxytocin 30 units added to 500 mL 5% Dextrose/Lactated Ringer's Recalled by...

The Issue: Subpotent Drug

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 1, 2017· Pharmedium Services, LLC

Recalled Item: Oxytocin 20 units added to 1000 mL Lactated Ringer's Injection Recalled by...

The Issue: Subpotent Drug

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 1, 2017· Pfizer Inc.

Recalled Item: Sterile Water for Injection Recalled by Pfizer Inc. Due to Non-Sterility:...

The Issue: Non-Sterility: cracked or chipped glass at the neck of Sterile Water for...

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

Class II — Potential Health HazardOngoing
Refund
FoodAugust 31, 2017· Reese Pharmaceutical Company

Recalled Item: Orange Flavor Immune Support Dietary Supplement Effervescent Tablets 10...

The Issue: The label does not list "Sodium" in the ingredient statement.

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

Class II — Potential Health HazardOngoing
Refund
FoodAugust 31, 2017· Reese Pharmaceutical Company

Recalled Item: Berry Flavor Immune Support Dietary Supplement Effervescent Tablets 10...

The Issue: The label does not list "Sodium" in the ingredient statement.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceAugust 31, 2017· DePuy Mitek, Inc., a Johnson & Johnson Co.

Recalled Item: 1113 Gravity Tube Set Pk/24 -SH Product Usage: The FMS Recalled by DePuy...

The Issue: Leakage of FMS gravity tub sets (281113) at the bulb and tube connection

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 31, 2017· Orthoscan, Inc.

Recalled Item: Mobile Mini C-arm system Part # 1000-0005. Intended to provide Recalled by...

The Issue: OrthoScan Inc. discovered during investigation of a non-standard work flow a...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 31, 2017· Orthoscan, Inc.

Recalled Item: Mobile Mini C-arm system Part # 1000-0004-FD. Intended to provide Recalled...

The Issue: OrthoScan Inc. discovered during investigation of a non-standard work flow a...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 31, 2017· Orthoscan, Inc.

Recalled Item: Mobile Mini C-arm system Part # 1000-0004. Intended to provide Recalled by...

The Issue: OrthoScan Inc. discovered during investigation of a non-standard work flow a...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 31, 2017· Siemens Medical Solutions USA, Inc

Recalled Item: Syngo.via systems with SW VB20A Recalled by Siemens Medical Solutions USA,...

The Issue: A software update was released on August 22, 2017. Performing this software...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 31, 2017· Orthoscan, Inc.

Recalled Item: Mobile Mini C-arm system Part # 1000-0001. Intended to provide Recalled by...

The Issue: OrthoScan Inc. discovered during investigation of a non-standard work flow a...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 30, 2017· Carl Zeiss Meditec AG

Recalled Item: Carl Zeiss INTRABEAM PRS 500 Recalled by Carl Zeiss Meditec AG Due to The...

The Issue: The device had an incorrect printed calibration value on the calibration...

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

Class II — Potential Health HazardOngoing
DrugAugust 30, 2017· Pfizer Inc.

Recalled Item: Vancomycin Hydrochloride for Injection Recalled by Pfizer Inc. Due to...

The Issue: Presence of Particulate Matter: glass particulate found in vial

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

Class I — Serious Health HazardOngoing
Refund
DrugAugust 30, 2017· Noven Pharmaceuticals, Inc.

Recalled Item: Daytrana (methylphenidate transdermal system) Delivers 15 mg over 9 hours...

The Issue: Defective Delivery System: Products no longer meet the release liner removal...

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

Class II — Potential Health HazardOngoing
Refund
DrugAugust 30, 2017· Noven Pharmaceuticals, Inc.

Recalled Item: Daytrana (methylphenidate transdermal system) Delivers 10 mg over 9 hours...

The Issue: Defective Delivery System: Products no longer meet the release liner removal...

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

Class II — Potential Health HazardOngoing
Refund