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. 2,486 recalls have been distributed to Oregon in the last 12 months.

50,914 total recalls
2,486 in last 12 months

Showing 2376123780 of 50,914 recalls

Medical DeviceJanuary 4, 2019· Cook Inc.

Recalled Item: Heavy Duty PTFE Wire Guide Recalled by Cook Inc. Due to The wire guide may...

The Issue: The wire guide may be incorrectly loaded into the wire guide holder, leading...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 4, 2019· Cook Inc.

Recalled Item: Percutaneous Malecot Nephrostomy Set Recalled by Cook Inc. Due to The wire...

The Issue: The wire guide may be incorrectly loaded into the wire guide holder, leading...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 4, 2019· Cook Inc.

Recalled Item: Percutaneous Pigtail Nephrostomy Set Recalled by Cook Inc. Due to The wire...

The Issue: The wire guide may be incorrectly loaded into the wire guide holder, leading...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 4, 2019· Cook Inc.

Recalled Item: Universa Soft Ureteral Stent Recalled by Cook Inc. Due to The wire guide may...

The Issue: The wire guide may be incorrectly loaded into the wire guide holder, leading...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 4, 2019· Cook Inc.

Recalled Item: Sof-Flex Multi-Lenqth Ureteral Stent Set Recalled by Cook Inc. Due to The...

The Issue: The wire guide may be incorrectly loaded into the wire guide holder, leading...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 4, 2019· Cook Inc.

Recalled Item: Fixed Core Straight Safety Wire Guide Recalled by Cook Inc. Due to The wire...

The Issue: The wire guide may be incorrectly loaded into the wire guide holder, leading...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 4, 2019· Wilson-Cook Medical Inc.

Recalled Item: Acusnare Polypectomy (Duck Bill Shaped) Snare Used with an electrosurgical...

The Issue: Complaints of the snare loop not completely retracting and/or misshaping of...

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

Class II — Potential Health HazardOngoing
DrugJanuary 3, 2019· Sun Pharmaceutical Industries, Inc.

Recalled Item: Vecuronium Bromide for Injection 20 mg* *1mg/mL when reconstituted to...

The Issue: Presence of Particulate Matter: Foreign matter identified as glass detected...

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

Class I — Serious Health HazardOngoing
Refund
DrugJanuary 3, 2019· Sun Pharmaceutical Industries, Inc.

Recalled Item: Vecuronium Bromide for Injection 10 mg* Recalled by Sun Pharmaceutical...

The Issue: Presence of Particulate Matter: Foreign matter identified as glass detected...

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

Class I — Serious Health HazardOngoing
Refund
FoodJanuary 3, 2019· Century Snacks LLC

Recalled Item: Snak Club Tajin Chili & Lime Peanuts Mild 5 oz. Recalled by Century Snacks...

The Issue: Undeclared allergen; tree nuts.

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 2, 2019· Baxter Healthcare Corporation

Recalled Item: Dianeal Low Calcium (2.5 mEq/L) Peritoneal Dialysis Solution with 1.5%...

The Issue: Lack of Assurance of Sterility: Confirmed customer complaints for leaks on...

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 2, 2019· Lupin Pharmaceuticals Inc.

Recalled Item: Cefdinir for Oral Suspension USP Recalled by Lupin Pharmaceuticals Inc. Due...

The Issue: CGMP Deviations: Product complaints received indicating reconstituted...

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 2, 2019· Heritage Pharmaceuticals, Inc.

Recalled Item: Cidofovir Injection 375mg/5mL (75mg/mL) vial injection. 5 mL vials Recalled...

The Issue: Lack of Assurance of Sterility: complaints received about dried powder on...

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

Class II — Potential Health HazardOngoing
Refund
DrugJanuary 2, 2019· Lupin Pharmaceuticals Inc.

Recalled Item: Cefdinir for Oral Suspension USP Recalled by Lupin Pharmaceuticals Inc. Due...

The Issue: CGMP Deviations: Product complaints received indicating reconstituted...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJanuary 2, 2019· Abbott Laboratories, Inc

Recalled Item: ARCHITECT MAGNESIUM Recalled by Abbott Laboratories, Inc Due to Abbott...

The Issue: Abbott internal testing has identified that the Magnesium urine application...

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

Class II — Potential Health HazardOngoing
Medical DeviceJanuary 2, 2019· Leica Microsystems, Inc.

Recalled Item: Leica M220 F12 surgical microscope The Leica M220 F12 surgical Recalled by...

The Issue: The M220 optics may unintentionally drop into the surgical field, risking...

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

Class II — Potential Health HazardOngoing
FoodDecember 31, 2018· Willamette Valley Pie Company, LLC.

Recalled Item: IQF Red Raspberries Recalled by Willamette Valley Pie Company, LLC. Due to...

The Issue: IQF Red Raspberries are recalled due to a potential contamination with...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceDecember 27, 2018· Cardinal Health 200, LLC

Recalled Item: Curity All Purpose Sponges Recalled by Cardinal Health 200, LLC Due to...

The Issue: Curity All Purpose Sponges were not sterilized and distributed

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 26, 2018· Luminex Corporation

Recalled Item: Vergene Amplification Tray - 700uL Recalled by Luminex Corporation Due to On...

The Issue: On lot of VERIGENE(R) BC-GP Utility Kits (20-011-018) were labeled with the...

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

Class III — Low RiskOngoing
Medical DeviceDecember 26, 2018· Steris Corporation

Recalled Item: ATLAS Loading Car Recalled by Steris Corporation Due to The ATLAS loading...

The Issue: The ATLAS loading car may not remain fully engaged with the latch on the...

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

Class II — Potential Health HazardOngoing