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. 2,454 recalls have been distributed to Oregon in the last 12 months.

50,914 total recalls
2,454 in last 12 months

Showing 3316133180 of 50,914 recalls

FoodAugust 30, 2016· Snyder's-Lance Inc.

Recalled Item: Diamond of California¿ Macadamia Halves and Pieces 2.25oz packages Recalled...

The Issue: Product may be potentially contaminated with Salmonella.

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

Class I — Serious Health HazardOngoing
Refund
FoodAugust 30, 2016· BIMBO Bakeries USA Inc.

Recalled Item: Entenmann's Little Bites Chocolate Chip Muffins Recalled by BIMBO Bakeries...

The Issue: Presence of plastic in muffins and brownies.

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

Class II — Potential Health HazardOngoing
Refund
FoodAugust 30, 2016· Snyder's-Lance Inc.

Recalled Item: Diamond of California¿ Chopped Macadamia Nuts 4oz Recalled by Snyder's-Lance...

The Issue: Product may be potentially contaminated with Salmonella.

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceAugust 30, 2016· ErgoSafe Products, LLC (DBA) Prism Medical

Recalled Item: Carry bar which is an accessory to a lift used Recalled by ErgoSafe...

The Issue: The black plastic puck on the carry bar is breaking resulting in potential...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 30, 2016· Siemens Healthcare Diagnostics, Inc.

Recalled Item: IMMULITE/ IMMULITE 1000 Systems CMM CMV IgM Assay Recalled by Siemens...

The Issue: Multiple customers reported seeing an increase in imprecision with some...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 30, 2016· Siemens Healthcare Diagnostics, Inc.

Recalled Item: IMMULITE 2000/IMMULITE 2000XPi Systems CMM CMV IgM Assay Recalled by Siemens...

The Issue: Multiple customers reported seeing an increase in imprecision with some...

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

Class II — Potential Health HazardOngoing
DrugAugust 29, 2016· Dr. Reddy's Laboratories, Inc.

Recalled Item: ZENATANE (isotretinoin capsules USP) 20 mg Recalled by Dr. Reddy's...

The Issue: Failed Dissolution Specifications

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

Class III — Low RiskOngoing
Refund
Medical DeviceAugust 29, 2016· Angiodynamics Inc. (Navilyst Medical Inc.)

Recalled Item: BioFlo PICC with ENDEXO and PASV Valve Technology Maximal Barrier Recalled...

The Issue: Medline Industries, Inc. supplies Navilyst with sterile package gloves...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 29, 2016· Angiodynamics Inc. (Navilyst Medical Inc.)

Recalled Item: BioFlo PICC with ENDEXO Technology Maximal Barrier Nursing Kit - Recalled by...

The Issue: Medline Industries, Inc. supplies Navilyst with sterile package gloves...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 29, 2016· Angiodynamics Inc. (Navilyst Medical Inc.)

Recalled Item: Xcela Power Injectable PICC Maximal Barrier Nursing Kit The Maximal Recalled...

The Issue: Medline Industries, Inc. supplies Navilyst with sterile package gloves...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 29, 2016· Smith & Nephew, Inc.

Recalled Item: TANDEM (TM) COCR SHELL UHMWPE LINER BIPOLAR Recalled by Smith & Nephew, Inc....

The Issue: Some Bipolar shells were manufactured with an out of specification retainer...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 29, 2016· Stryker Howmedica Osteonics Corp.

Recalled Item: LFIT Anatomic V40 Femoral Head Recalled by Stryker Howmedica Osteonics Corp....

The Issue: Stryker received several complaints describing incidence of harm secondary...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 29, 2016· Smith & Nephew, Inc.

Recalled Item: TANDEM (TM) INTL COCR SHELL UHMWPE LINER BIPOLAR Recalled by Smith & Nephew,...

The Issue: Some Bipolar shells were manufactured with an out of specification retainer...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 29, 2016· LDR Spine USA, Inc.

Recalled Item: ROI-A Anterior Delivery Device. Orthopedic manual surgical instrument. Model...

The Issue: The ROI-A Anterior Delivery Device T-Handle, part number SI-ROIA-0023 has...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 29, 2016· ConMed Corporation

Recalled Item: CONCEPT HEATWAVE Electrode 130 mm x 2.3 mm diameter Recalled by ConMed...

The Issue: CONMED received complaints of damage to the CS-023 electrodes shaft...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 29, 2016· Trimed Inc

Recalled Item: TriMed Semi-Tubular Plate Recalled by Trimed Inc Due to TriMed is recalling...

The Issue: TriMed is recalling the Semi-Tubular Plates with 10 holes (SMTP-10) because...

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

Class II — Potential Health HazardOngoing
FoodAugust 26, 2016· Complete Packaging & Manufacturing, LLC

Recalled Item: Dietary Supplement Acidophilus Blend Recalled by Complete Packaging &...

The Issue: Nature's Power Solutions Acidophilus Blend due to undeclared milk allergen.

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceAugust 26, 2016· Teleflex Medical

Recalled Item: Willy Rusch GmbH Tracheostomy Tube Set Cannulation of tracheotomised...

The Issue: The connector may disconnect from the tracheostomy tube during use.

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 26, 2016· Abbott Medical Optics Inc. (AMO)

Recalled Item: TECNIS OptiBlue 1-Piece Intraocular Lens (IOL) Recalled by Abbott Medical...

The Issue: Abbott Medical Optics is recalling Intraocular Lenses (IOLs) because they...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 26, 2016· The Anspach Effort, Inc.

Recalled Item: G1 Dissection Tool - 3mm CRS DBALL Recalled by The Anspach Effort, Inc. Due...

The Issue: The firm discovered on March 4, 2016 that several product codes were...

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

Class II — Potential Health HazardOngoing