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. 2,433 recalls have been distributed to Washington in the last 12 months.

51,768 total recalls
2,433 in last 12 months

Showing 4854148560 of 51,768 recalls

Medical DeviceMarch 18, 2013· Clorox Healthcare Holdings, LLC (dba HealthLink)

Recalled Item: HealthLink***BIOPSY PUNCHES*** Disposable manual instrument for skin biopsy....

The Issue: Due to lack of sterilization.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 18, 2013· Clorox Healthcare Holdings, LLC (dba HealthLink)

Recalled Item: ARGENT SURGICAL SYSTEMS***BIOPSY Punches*** Disposable manual instrument for...

The Issue: Due to lack of sterilization.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 18, 2013· Shimadzu Medical Systems

Recalled Item: Shimadzu Corporation - Mobile DaRt Evolution This device is a Recalled by...

The Issue: The recall was initiated because Shimadzu Corporation has identified a...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 18, 2013· Linvatec Corp. dba ConMed Linvatec

Recalled Item: HD Still Capture System ConMed Linvatec . Captures Recalled by Linvatec...

The Issue: The VP1600 HD Still Capture Image System is recalled due to an anomaly...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 18, 2013· LeMaitre Vascular, Inc.

Recalled Item: LeMaitre Stent Guide: 1102-00 (100 strips) Recalled by LeMaitre Vascular,...

The Issue: Devices were not sealed correctly during the manufacturing process, and the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 18, 2013· Hospira Inc.

Recalled Item: GemStar Pump - Battery Product Usage: The GemStar Pump is Recalled by...

The Issue: Battery level lower then 2.4 volts results in corrupt history log and loss...

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 18, 2013· Hospira Inc.

Recalled Item: The GemStar Pump is a small and lightweight Recalled by Hospira Inc. Due to...

The Issue: Pump shutting off during use without warning.

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 18, 2013· NxStage Medical, Inc.

Recalled Item: NxStage PureFlow-B Solution Recalled by NxStage Medical, Inc. Due to Mislabeling

The Issue: Product may be mislabeled.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 18, 2013· Hospira Inc.

Recalled Item: The GemStar Pump is a small and lightweight Recalled by Hospira Inc. Due to...

The Issue: Pump shutting off during use without warning.

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 18, 2013· Hospira Inc.

Recalled Item: GemStar Pump - Battery Product Usage: The GemStar Pump is Recalled by...

The Issue: Battery level lower then 2.4 volts results in corrupt history log and loss...

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

Class I — Serious Health HazardOngoing
Medical DeviceMarch 18, 2013· LeMaitre Vascular, Inc.

Recalled Item: Glow 'N Tell 20 cm Tape: 1100-00 (100 strips) Recalled by LeMaitre Vascular,...

The Issue: Devices were not sealed correctly during the manufacturing process, and the...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 18, 2013· Integra Burlington MA, Inc.

Recalled Item: Integra Ojemann Cortical Stimulator Recalled by Integra Burlington MA, Inc....

The Issue: If the headphone jack is in use during a surgical procedure with the OCS2...

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

Class II — Potential Health HazardOngoing
DrugMarch 16, 2013· Tarmac Products, Inc. d.b.a. Axara Pharmaceuticals

Recalled Item: "Well at Wallgreens" Regular Strength Antacid Liquid...

The Issue: Microbial Contamination of Non-Sterile Products: Lot in question had an...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 15, 2013· Teva Pharmaceuticals USA, Inc.

Recalled Item: Lessina(R) (Levonorgestrel and ethinyl estradiol tablets Recalled by Teva...

The Issue: Failed Impurity/Degradation Specification; an impurity identified as...

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

Class III — Low RiskOngoing
Refund
DrugMarch 15, 2013· Teva Pharmaceuticals USA, Inc.

Recalled Item: Errin (norethindrone tablets Recalled by Teva Pharmaceuticals USA, Inc. Due...

The Issue: Failed Impurity/Degradation Specification; an impurity identified as...

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

Class III — Low RiskOngoing
Refund
DrugMarch 15, 2013· Teva Pharmaceuticals USA, Inc.

Recalled Item: Junel(TM) Fe 1.5/30 (norethindrone acetate and ethinyl estradiol tablets...

The Issue: Failed Impurity/Degradation Specification; an impurity identified as...

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

Class III — Low RiskOngoing
Refund
DrugMarch 15, 2013· Teva Pharmaceuticals USA, Inc.

Recalled Item: Camila (norethindrone tablets Recalled by Teva Pharmaceuticals USA, Inc. Due...

The Issue: Failed Impurity/Degradation Specification; an impurity identified as...

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

Class III — Low RiskOngoing
Refund
DrugMarch 15, 2013· Teva Pharmaceuticals USA, Inc.

Recalled Item: Jolessa(R) (levonorgestrel/ethinyl estradiol tablets Recalled by Teva...

The Issue: Failed Impurity/Degradation Specification; an impurity identified as...

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

Class III — Low RiskOngoing
Refund
DrugMarch 15, 2013· Teva Pharmaceuticals USA, Inc.

Recalled Item: Balziva(TM) (norethindrone and ethinyl estradiol tablets Recalled by Teva...

The Issue: Failed Impurity/Degradation Specification; an impurity identified as...

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

Class III — Low RiskOngoing
Refund
Medical DeviceMarch 15, 2013· MCKESSON TECHNOLOGIES INC.

Recalled Item: McKesson Anesthesia Care Product Usage: The McKesson Anesthesia Care system...

The Issue: There was an occurrence where the patient case data did not match the...

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

Class I — Serious Health HazardOngoing