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. 2,486 recalls have been distributed to Washington in the last 12 months.

51,768 total recalls
2,486 in last 12 months

Showing 4196141980 of 51,768 recalls

Medical DeviceNovember 21, 2014· Smiths Medical ASD, Inc.

Recalled Item: Hypodermic Needle Pro¿ Edge" Safety Device with Syringe 20G x1 Recalled by...

The Issue: Needle is not captured in the needle safety sheath in specific lots.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 21, 2014· Instrumentation Laboratory Co.

Recalled Item: HemosIL PT-Fibrinogen HS PLUS Recalled by Instrumentation Laboratory Co. Due...

The Issue: Some vials of HemosIL PT-Fibrinogen HS PLUS, Part No. 0008469810 (various...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 21, 2014· Smiths Medical ASD, Inc.

Recalled Item: Hypodermic Needle Pro¿ Edge" Safety Device with Syringe 20G x1 Recalled by...

The Issue: Needle is not captured in the needle safety sheath in specific lots.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 21, 2014· Intuitive Surgical, Inc.

Recalled Item: Fluorescence Imaging Procedure Kit Recalled by Intuitive Surgical, Inc. Due...

The Issue: The storage conditions for indocyanine green (ICG) are not on the individual...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 21, 2014· Intuitive Surgical, Inc.

Recalled Item: Fluorescence Imaging Procedure Kit Recalled by Intuitive Surgical, Inc. Due...

The Issue: The storage conditions for indocyanine green (ICG) are not on the individual...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 21, 2014· Zimmer Manufacturing B.V.

Recalled Item: Bone Screw Recalled by Zimmer Manufacturing B.V. Due to Analysis of returned...

The Issue: Analysis of returned complaint devices, product in inventory, and device...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 21, 2014· TomoTherapy Incorporated

Recalled Item: TomoTherapy Treatment System with software versions 2.0.1 / 2.0.2 / Recalled...

The Issue: Accuray has become aware of a potential safety issue related to the...

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

Class II — Potential Health HazardOngoing
DrugNovember 20, 2014· One and Zen

Recalled Item: GINSENG KIANPI PIL Recalled by One and Zen Due to Undeclared Dexamethasone

The Issue: Marketed Without An Approved NDA/ANDA: FDA analysis found this product to...

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

Class II — Potential Health HazardOngoing
Refund
FoodNovember 20, 2014· Evershing International Trading Inc.

Recalled Item: Wake-Up Instant Coffee Mix (weasel coffee) Melange de Cafe Instantane...

The Issue: Firm was notified by CFIA and FDA that CFIA testing found undeclared milk...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceNovember 20, 2014· Philips Medical Systems, Inc.

Recalled Item: Lithium Polymer Fiber Optic Module Batteries used in the Intera Recalled by...

The Issue: VCG battery ignited in a VCG unit when recharging.

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 20, 2014· Phadia US Inc

Recalled Item: Phadia 1000 Instrument (introduced as UniCAP 1000) Recalled by Phadia US Inc...

The Issue: During an investigation of instrument logs it was determined that In...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 20, 2014· Roche Diagnostics Operations, Inc.

Recalled Item: ACCU-CHEK Tender II 13/110 10 + 10 pieces Product Usage: Recalled by Roche...

The Issue: Roche Diabetes Care was informed by UnoMedical, the Manufacturer of...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 20, 2014· Roche Diagnostics Operations, Inc.

Recalled Item: ACCU-CHEK Tender I 17/80 10 pieces Product Usage: Intended for Recalled by...

The Issue: Roche Diabetes Care was informed by UnoMedical, the Manufacturer of...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 20, 2014· Roche Diagnostics Operations, Inc.

Recalled Item: ACCU-CHEK Tender II 17/80 10 + 10 pieces Product Usage: Recalled by Roche...

The Issue: Roche Diabetes Care was informed by UnoMedical, the Manufacturer of...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 20, 2014· Roche Diagnostics Operations, Inc.

Recalled Item: ACCU-CHEK Tender I 17/60 10 pieces Product Usage: Intended for Recalled by...

The Issue: Roche Diabetes Care was informed by UnoMedical, the Manufacturer of...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 20, 2014· Roche Diagnostics Operations, Inc.

Recalled Item: ACCU-CHEK¿ Tender I 13/60 10 pieces Product Usage: Usage: Intended Recalled...

The Issue: Roche Diabetes Care was informed by UnoMedical, the Manufacturer of...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 20, 2014· Roche Diagnostics Operations, Inc.

Recalled Item: ACCU-CHEK Tender II 13/80 10 + 10 pieces Product Usage: Recalled by Roche...

The Issue: Roche Diabetes Care was informed by UnoMedical, the Manufacturer of...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 20, 2014· Roche Diagnostics Operations, Inc.

Recalled Item: ACCU-CHEK Tender I 17/110 10 pieces Product Usage: Intended for Recalled by...

The Issue: Roche Diabetes Care was informed by UnoMedical, the Manufacturer of...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 20, 2014· Roche Diagnostics Operations, Inc.

Recalled Item: ACCU-CHEK Tender II 17/110 10 + 10 pieces Product Usage: Recalled by Roche...

The Issue: Roche Diabetes Care was informed by UnoMedical, the Manufacturer of...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 20, 2014· Roche Diagnostics Operations, Inc.

Recalled Item: ACCU-CHEK Tender II 17/60 10 + 10 pieces Product Usage: Recalled by Roche...

The Issue: Roche Diabetes Care was informed by UnoMedical, the Manufacturer of...

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

Class II — Potential Health HazardOngoing