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. 2,640 recalls have been distributed to Washington in the last 12 months.

51,768 total recalls
2,640 in last 12 months

Showing 2534125360 of 51,768 recalls

Medical DeviceSeptember 10, 2018· Howmedica Osteonics Corp.

Recalled Item: Sterile Knee Instruments Disposable Fluted Headless Pins Recalled by...

The Issue: Potential for outer pouch sterile barrier to be compromised

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 10, 2018· Boston Scientific Corporation

Recalled Item: Model 3300 LATITUDE(TM) Programming System Product Usage - The Boston...

The Issue: There is a potential for the Pacing System Analyzer (PSA) to exhibit...

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

Class II — Potential Health HazardOngoing
DrugSeptember 7, 2018· Noven Pharmaceuticals, Inc.

Recalled Item: Minivelle (estradiol transdermal system) Patches Recalled by Noven...

The Issue: Defective Delivery System: out of specification results for shear, an...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 7, 2018· Noven Pharmaceuticals, Inc.

Recalled Item: Minivelle (estradiol transdermal system) Patches Delivers 0.1 mg/day...

The Issue: Defective Delivery System: out of specification results for shear, an...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 7, 2018· Noven Pharmaceuticals, Inc.

Recalled Item: Minivelle (estradiol transdermal system) Patches Recalled by Noven...

The Issue: Defective Delivery System: out of specification results for shear, an...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 7, 2018· Noven Pharmaceuticals, Inc.

Recalled Item: Minivelle (estradiol transdermal system) Patches Recalled by Noven...

The Issue: Defective Delivery System: out of specification results for shear, an...

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

Class II — Potential Health HazardOngoing
Refund
FoodSeptember 7, 2018· Shearers Foods, Llc

Recalled Item: White Corn Tortilla Chips packaged under the following brand names Recalled...

The Issue: Corn Chip products are being recalled due to possible metal contamination.

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

Class II — Potential Health HazardOngoing
Refund
FoodSeptember 7, 2018· Shearers Foods, Llc

Recalled Item: Yellow Corn Tortilla Chips packaged under the following brand names Recalled...

The Issue: Corn Chip products are being recalled due to possible metal contamination.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceSeptember 7, 2018· Vital Scientific N.V.

Recalled Item: V-Twin Recalled by Vital Scientific N.V. Due to The action is being...

The Issue: The action is being initiated because the cooling indicator board was...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 7, 2018· Abbott Laboratories, Inc

Recalled Item: APS Accelerator modular systems Recalled by Abbott Laboratories, Inc Due to...

The Issue: The firm identified customer sites where modules which the safety pacemaker...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 7, 2018· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Dimension Vista Lipase Flex Reagent Cartridge Recalled by Siemens Healthcare...

The Issue: There is lot to lot variability for QC and patient results when using the...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 7, 2018· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Dimension Lipase Flex Reagent Cartridge Recalled by Siemens Healthcare...

The Issue: There is lot to lot variability for QC and patient results when using the...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 7, 2018· Bayer Medical Care, Inc.

Recalled Item: Codan Filter (Codan catalog number BC 693) used with Medrad Recalled by...

The Issue: Bayer has received reports of loose particulate in the filter when the dust...

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

Class II — Potential Health HazardOngoing
DrugSeptember 6, 2018· InvaGen Pharmaceuticals, Inc.

Recalled Item: Bupropion Hydrochloride ER Tablets Recalled by InvaGen Pharmaceuticals, Inc....

The Issue: Failed impurities/ degradation specifications: Out-of-specification results...

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

Class III — Low RiskOngoing
Refund
DrugSeptember 6, 2018· Baxter Healthcare Corporation

Recalled Item: 0.9% Sodium Chloride Injection USP 50 mL Viaflex container Baxter Recalled...

The Issue: cGMP Deviation

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 6, 2018· Par Pharmaceutical, Inc.

Recalled Item: Pramipexole dihydrochloride extended release tablets Recalled by Par...

The Issue: Failed impurities/degradation specifications: Finished product contain a...

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

Class III — Low RiskOngoing
Refund
Medical DeviceSeptember 6, 2018· Stihler Electronic Gmbh

Recalled Item: Heating Profile PRISMAFLO II S blood return warmer for Prismaflex Recalled...

The Issue: PRISMAFLO II and PRISMAFLO II S Heating Profile only and not the Control...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 6, 2018· Stihler Electronic Gmbh

Recalled Item: Heating Profile PRISMAFLO II S blood return warmer for Prismaflex Recalled...

The Issue: PRISMAFLO II and PRISMAFLO II S Heating Profile only and not the Control...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 6, 2018· Stihler Electronic Gmbh

Recalled Item: Heating Profile PRISMAFLO II blood return warmer for Prismaflex Product...

The Issue: PRISMAFLO II and PRISMAFLO II S Heating Profile only and not the Control...

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

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 6, 2018· Stryker Medical Division of Stryker Corporation

Recalled Item: Altrix¿ Precision Temperature Management System Model: 8001Product Usage:...

The Issue: Users may experience alarm fatigue due to frequent alarming relating to...

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

Class II — Potential Health HazardOngoing