Product Recalls in Oregon

Product recalls affecting Oregon — including food, drugs, consumer products, medical devices, and vehicles distributed to Oregon. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 1,733 recalls have been distributed to Oregon in the last 12 months.

50,914 total recalls
1,733 in last 12 months

Showing 4380143820 of 50,914 recalls

Medical DeviceMarch 20, 2014· Global Cooling Inc

Recalled Item: Stirling Ultracold Portable Shuttle Recalled by Global Cooling Inc Due to...

The Issue: The external power supply input is overheating at the connection to the freezer.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 20, 2014· Alere San Diego, Inc.

Recalled Item: Alere Triage BNP Test for the Beckman Coulter Access Family Recalled by...

The Issue: These lots may not recover within range when tested using certain...

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

Class II — Potential Health HazardOngoing
DrugMarch 20, 2014· Caraco Pharmaceutical Laboratories, Ltd.

Recalled Item: Venlafaxine Hydrochloride Extended-Release Tablets Recalled by Caraco...

The Issue: Failed Dissolution Specifications: Stability results found the product did...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 20, 2014· Apotex Inc.

Recalled Item: Risperidone Oral Solution Recalled by Apotex Inc. Due to Failed...

The Issue: Failed Impurities/Degradation Specifications: Out of Specification for an...

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

Class III — Low RiskOngoing
Refund
DrugMarch 20, 2014· Caraco Pharmaceutical Laboratories, Ltd.

Recalled Item: Venlafaxine Hydrochloride Extended-Release Tablets Recalled by Caraco...

The Issue: Failed Dissolution Specifications: Stability results found the product did...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMarch 19, 2014· Zimmer, Inc.

Recalled Item: Tennis Elbow Support Recalled by Zimmer, Inc. Due to During a transfer of...

The Issue: During a transfer of products from a recently shutdown facility, the firm...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 19, 2014· Zimmer, Inc.

Recalled Item: Hinged Knee Support***LATEX FREE" Product Usage: Provide added lateral...

The Issue: During a transfer of products from a recently shutdown facility, the firm...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 19, 2014· Zimmer, Inc.

Recalled Item: DROP LOK" Knee Brace***LATEX FREE" Product Usage: Used in the treatment...

The Issue: During a transfer of products from a recently shutdown facility, the firm...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 19, 2014· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Dimension Vista¿ CSA and CSAE The Cyclosporine method is an Recalled by...

The Issue: A complaint was received of Dimension Vista¿ CSA and CSAE under-recovery of...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 19, 2014· Zimmer, Inc.

Recalled Item: Cartilage Knee Brace***LATEX FREE" Product Usage: Used in the treatment...

The Issue: During a transfer of products from a recently shutdown facility, the firm...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 19, 2014· CareFusion 303, Inc.

Recalled Item: SmartSite Extension Set Recalled by CareFusion 303, Inc. Due to...

The Issue: Disconnections and leakages at the connection of the smallbore tubing and...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 18, 2014· SCM True Air Technologies LLC

Recalled Item: ECATS E 850 Bariatric Bed Recalled by SCM True Air Technologies LLC Due to...

The Issue: The firm is recalling the products due to lack of design controls, lack of a...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 18, 2014· SCM True Air Technologies LLC

Recalled Item: MaXair True Low Air Loss Mattress Replacement System Recalled by SCM True...

The Issue: The firm is recalling the products due to lack of design controls, lack of a...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 18, 2014· Energizer Personal Care

Recalled Item: Playtex Nurser Deluxe Double Electric Breast Pump Recalled by Energizer...

The Issue: Some of the power adapters outer casings may become loose and separate,...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 18, 2014· Stryker Instruments Div. of Stryker Corporation

Recalled Item: 2.5MM Aggressive Blade Known as a Sinuscopic Shaver Blade Recalled by...

The Issue: Stryker Instruments is voluntarily recalling the single use 2.5MM Aggressive...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 18, 2014· SCM True Air Technologies LLC

Recalled Item: JK Bariatric Beds Recalled by SCM True Air Technologies LLC Due to The firm...

The Issue: The firm is recalling the products due to lack of design controls, lack of a...

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

Class II — Potential Health HazardOngoing
DrugMarch 18, 2014· Glenmark Generics Inc., USA

Recalled Item: Ranitidine Tablets USP Recalled by Glenmark Generics Inc., USA Due to...

The Issue: Presence of Foreign Tablets/Capsules: Recall is due to a pharmacist...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMarch 17, 2014· 3M Company - Health Care Business

Recalled Item: 3M" Steri-Vac" Gas Sterilizer/Aerators Recalled by 3M Company - Health Care...

The Issue: Recently, 3M received a single report of a potential exposure to Ethylene...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 17, 2014· Philips Medical Systems, Inc.

Recalled Item: Digital Diagnost Recalled by Philips Medical Systems, Inc. Due to The...

The Issue: The footboard of Patient support for stitching can be fixed in upper...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 17, 2014· Stryker Communications

Recalled Item: BAM (SHAPE) ARM Recalled by Stryker Communications Due to During the use of...

The Issue: During the use of the SHAPE Arm there is the potential for the monitor mount...

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

Class II — Potential Health HazardOngoing