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 3050130520 of 51,768 recalls

Medical DeviceJune 1, 2017· Shippert Medical Technologies

Recalled Item: Tissu-Trans Filtron 500 Recalled by Shippert Medical Technologies Due to...

The Issue: Seal integrity of the Tissu-Trans product sterile packages cannot be assured.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 1, 2017· Shippert Medical Technologies

Recalled Item: Tissu-Trans Filtron 250 Recalled by Shippert Medical Technologies Due to...

The Issue: Seal integrity of the Tissu-Trans product sterile packages cannot be assured.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 1, 2017· Shippert Medical Technologies

Recalled Item: Tissu-Trans MEGA 1500 Recalled by Shippert Medical Technologies Due to Seal...

The Issue: Seal integrity of the Tissu-Trans product sterile packages cannot be assured.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 1, 2017· Shippert Medical Technologies

Recalled Item: Tissu-Trans SFILL 360 Recalled by Shippert Medical Technologies Due to Seal...

The Issue: Seal integrity of the Tissu-Trans product sterile packages cannot be assured.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 1, 2017· Arrow International Inc

Recalled Item: ARROW¿ PICC powered by ARROW¿ VPS¿ Stylet The Pressure Injectable Recalled...

The Issue: There is a possibility that the finished good kits may contain 5 Fr...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 1, 2017· Arrow International Inc

Recalled Item: Arrow(R) VPS(R) Access Kit for use with 4 Fr. Peripherally Recalled by Arrow...

The Issue: There is a possibility that the finished good kits may contain 5 Fr...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 1, 2017· Arrow International Inc

Recalled Item: ArrowADVANTAGE5" Pressure Injectable Peripherally Inserted Central Catheter...

The Issue: There is a possibility that the finished good kits may contain 5 Fr...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 1, 2017· Arrow International Inc

Recalled Item: ARROW¿ PICC powered by ARROW¿ VPS¿ Stylet The Pressure Injectable Recalled...

The Issue: There is a possibility that the finished good kits may contain 5 Fr...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 1, 2017· Shippert Medical Technologies

Recalled Item: Tissu-Trans Filtron 1000 Recalled by Shippert Medical Technologies Due to...

The Issue: Seal integrity of the Tissu-Trans product sterile packages cannot be assured.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 1, 2017· Shippert Medical Technologies

Recalled Item: Tissu-Trans Filtron 100 Recalled by Shippert Medical Technologies Due to...

The Issue: Seal integrity of the Tissu-Trans product sterile packages cannot be assured.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 1, 2017· Shippert Medical Technologies

Recalled Item: Tissu-Trans Filtron 2000 Recalled by Shippert Medical Technologies Due to...

The Issue: Seal integrity of the Tissu-Trans product sterile packages cannot be assured.

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 1, 2017· Intuitive Surgical, Inc.

Recalled Item: da Vinci Xi Surgical System Product Usage: The da Vinci Recalled by...

The Issue: da Vinci Xi(R) Surgical System Patient Side Carts (PSC) were shipped to the...

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

Class II — Potential Health HazardOngoing
DrugJune 1, 2017· American Pharmaceutical Ingredients LLC

Recalled Item: Doxycycline Hyclate USP Recalled by American Pharmaceutical Ingredients LLC...

The Issue: Labeling: Not Elsewhere Classified. Manufacturer and product were discovered...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 1, 2017· L. Perrigo Company

Recalled Item: Option 2 Recalled by L. Perrigo Company Due to Defective Container: Carton...

The Issue: Defective Container: Carton is missing the tablet blister strip and tablet.

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 1, 2017· Lucid Pharma LLC

Recalled Item: Venlafaxine Hydrochloride Extended-Release Capsules USP Recalled by Lucid...

The Issue: Failed Tablet/Capsules Specifications: pharmacists complaints for bottles...

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

Class II — Potential Health HazardOngoing
Refund
DrugMay 31, 2017· Teva Pharmaceuticals

Recalled Item: Paliperidone Extended-Release Tablets Recalled by Teva Pharmaceuticals Due...

The Issue: Failed Dissolution Specifications: Drug release test result, obtained during...

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

Class I — Serious Health HazardOngoing
Refund
FoodMay 31, 2017· Blue Diamond Growers

Recalled Item: Blue Diamond Almonds Blanc DCD FN C (blanched diced fine) Recalled by Blue...

The Issue: Firm was notified by customer of a positive Salmonella result obtained when...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceMay 31, 2017· Encore Medical, Lp

Recalled Item: 3DKNEE(TM) SYSTEM e+ Recalled by Encore Medical, Lp Due to Mis-pack. A size...

The Issue: Mis-pack. A size 6 Left 3DKnee Tibial Insert box and pouch contained a Size...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 31, 2017· Encore Medical, Lp

Recalled Item: 3DKNEE(TM) SYSTEM e+ Recalled by Encore Medical, Lp Due to Mis-pack. A size...

The Issue: Mis-pack. A size 6 Left 3DKnee Tibial Insert box and pouch contained a Size...

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

Class II — Potential Health HazardOngoing
Medical DeviceMay 31, 2017· Becton Dickinson & Company

Recalled Item: BD Precision Glide Needle 18G x 1 RB Recalled by Becton Dickinson & Company...

The Issue: Hub damage resulting in breakage and/or leakage during use.

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

Class II — Potential Health HazardOngoing