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. 2,420 recalls have been distributed to Oregon in the last 12 months.

50,914 total recalls
2,420 in last 12 months

Showing 4078140800 of 50,914 recalls

FoodDecember 2, 2014· House Of Flavors, Inc.

Recalled Item: Dark Cocoa Sorbetto packed in 14 oz. plastic jars Recalled by House Of...

The Issue: Undeclared milk was found in 14 oz. Dark Cocoa Sorbetto gelato manufactured...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceDecember 2, 2014· Siemens Medical Solutions USA, Inc

Recalled Item: Siemens Linear Accelerator: ARTISTE Recalled by Siemens Medical Solutions...

The Issue: Use of any unauthorized third-party components on Siemens LINACs may lead to...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 29, 2014· Vyaire Medical

Recalled Item: Adult AirLife dual-limb Recalled by Vyaire Medical Due to Manufacturing...

The Issue: Manufacturing error in humidification chamber may cause an overfill/overflow...

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 29, 2014· Vyaire Medical

Recalled Item: Infant AirLife single-limb Recalled by Vyaire Medical Due to Manufacturing...

The Issue: Manufacturing error in humidification chamber may cause an overfill/overflow...

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 29, 2014· Vyaire Medical

Recalled Item: Infant AirLife Dual- Recalled by Vyaire Medical Due to Manufacturing error...

The Issue: Manufacturing error in humidification chamber may cause an overfill/overflow...

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 29, 2014· Vyaire Medical

Recalled Item: Adult Air-Life single-limb circuit (Model AH202) with AirLife Humidification...

The Issue: Manufacturing error in humidification chamber may cause an overfill/overflow...

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 29, 2014· Magellan Diagnostics, Inc.

Recalled Item: Magellan Diagnostics LeadCare Ultra Blood Analyzer Part Number: 80-0010...

The Issue: LeadCare Plus and LeadCare Ultra Blood Lead Testing Systems may generate...

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

Class I — Serious Health HazardOngoing
Medical DeviceNovember 29, 2014· Magellan Diagnostics, Inc.

Recalled Item: Magellan Diagnostics LeadCare Ultra Blood Lead Test Kits Part Number:...

The Issue: LeadCare Plus and LeadCare Ultra Blood Lead Testing Systems may generate...

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

Class I — Serious Health HazardOngoing
FoodNovember 28, 2014· The Santa Barbara Smokehouse, Inc.

Recalled Item: Cambridge House Balmoral Thinly Sliced Exceptional Ready to Enjoy Smoked...

The Issue: The firm was notified by two customers of two lot/batch numbers testing...

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

Class I — Serious Health HazardOngoing
Refund
DrugNovember 26, 2014· Zydus Pharmaceuticals USA Inc

Recalled Item: Benzonatate Capsules Recalled by Zydus Pharmaceuticals USA Inc Due to Failed...

The Issue: Failed Tablet/Capsule Specifications: Recall due to wet and/or leaking capsules.

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

Class II — Potential Health HazardOngoing
Refund
FoodNovember 26, 2014· fgf brands, inc

Recalled Item: Mini Naan Eight (8) nann packaged in coated paper printed Recalled by fgf...

The Issue: The products were shipped without labels declaring the nutrition and...

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

Class II — Potential Health HazardOngoing
Refund
FoodNovember 26, 2014· High Quality Organics, Inc.

Recalled Item: Organic Cilantro Medium Bulk - size is dependent on customer request...

The Issue: Immediate customer received a positive result for Salmonella of Organic...

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceNovember 26, 2014· SCC Soft Computer

Recalled Item: SoftPath Laboratory Information System. Versions 4.3.0.8 Recalled by SCC...

The Issue: Modifications to diagnostic text may be: 1) Saved to the database but not...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 26, 2014· Lacrimedics Inc

Recalled Item: VisiPlugST for the Lacrimal Efficiency Test. It is also sold Recalled by...

The Issue: Moisture level may cause the VisiPlugST (or CollaSyn Plugs) to break apart,...

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

Class III — Low RiskOngoing
Medical DeviceNovember 26, 2014· Getinge Disinfection Ab

Recalled Item: GETINGE 46-SERIES Medical Washer-Disinfector Recalled by Getinge...

The Issue: Getinge Disinfection AB received complaints regarding sediment residuals in...

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

Class II — Potential Health HazardOngoing
DrugNovember 25, 2014· Hospira Inc.

Recalled Item: Dacarbazine Recalled by Hospira Inc. Due to Discoloration: Reconstituted...

The Issue: Discoloration: Reconstituted solution may appear pink instead of colorless...

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

Class III — Low RiskOngoing
Refund
DrugNovember 25, 2014· Baxter Healthcare Corp.

Recalled Item: Clinimix E 4.25/10 sulfite-free (4.25% Amino Acid with Electrolytes in...

The Issue: Lack of Assurance of Sterility; leaks were observed from the bag seam and...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceNovember 25, 2014· St Jude Medical

Recalled Item: TactiSys Quartz Pack Recalled by St Jude Medical Due to A configuration...

The Issue: A configuration update needs to be done on TactiSys to appropriately...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 25, 2014· Zimmer, Inc.

Recalled Item: Zimmer PERSONA Tibial Articular Surface Inserter Recalled by Zimmer, Inc....

The Issue: Potential for fracture of the tip of the product. The fractured tip is...

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

Class II — Potential Health HazardOngoing
Medical DeviceNovember 25, 2014· Carestream Health Inc

Recalled Item: DRX-Revolution Mobile X-Ray System Recalled by Carestream Health Inc Due to...

The Issue: While servicing a unit at a customer site, a field engineer discovered a...

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

Class II — Potential Health HazardOngoing