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. 1,020 recalls have been distributed to Oregon in the last 12 months.

50,914 total recalls
1,020 in last 12 months

Showing 29701–29720 of 50,914 recalls

Medical DeviceJune 7, 2017· Terumo Medical Corp

Recalled Item: Glidesheath Slender Hydrophilic Coated Introducer Sheath Recalled by Terumo...

The Issue: An incomplete seal at the chevron end of the primary packaging of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 7, 2017· Terumo Medical Corp

Recalled Item: Glidesheath Slender Hydrophilic Coated Introducer Sheath Recalled by Terumo...

The Issue: An incomplete seal at the chevron end of the primary packaging of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 7, 2017· Cenorin, LLC

Recalled Item: ThermaSure(TM) Recalled by Cenorin, LLC Due to Dryer unit not heating....

The Issue: Dryer unit not heating. Manufacturing issue causes the terminal block to...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 7, 2017· Philips Medical Systems (Cleveland) Inc

Recalled Item: Brilliance Big Bore Radiology CT (Model No. 728244) software version...

The Issue: It was reported that scanners running certain software versions provide...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 7, 2017· Terumo Medical Corp

Recalled Item: Glidesheath Slender Hydrophilic Coated Introducer Sheath A-Kit Recalled by...

The Issue: An incomplete seal at the chevron end of the primary packaging of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 7, 2017· Philips Medical Systems (Cleveland) Inc

Recalled Item: Ingenuity CT (Model No. 728326) Recalled by Philips Medical Systems...

The Issue: It was reported that scanners running certain software versions provide...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 7, 2017· Philips Medical Systems (Cleveland) Inc

Recalled Item: Ingenuity Core 128 (Model No. 728323) Recalled by Philips Medical Systems...

The Issue: It was reported that scanners running certain software versions provide...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 7, 2017· Terumo Medical Corp

Recalled Item: Glidesheath Slender Hydrophilic Coated Introducer Sheath A-Kit Recalled by...

The Issue: An incomplete seal at the chevron end of the primary packaging of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 7, 2017· Philips Medical Systems (Cleveland) Inc

Recalled Item: Brilliance 64 (Model No. 728231) Recalled by Philips Medical Systems...

The Issue: It was reported that scanners running certain software versions provide...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 7, 2017· Terumo Medical Corp

Recalled Item: Glidesheath Slender Hydrophilic Coated Introducer Sheath Recalled by Terumo...

The Issue: An incomplete seal at the chevron end of the primary packaging of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 7, 2017· Terumo Medical Corp

Recalled Item: Glidesheath Slender Hydrophilic Coated Introducer Sheath Recalled by Terumo...

The Issue: An incomplete seal at the chevron end of the primary packaging of the...

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

Class II — Potential Health HazardOngoing
FoodJune 7, 2017· Lyrical Foods Inc

Recalled Item: Kite Hill Almond Yogurt Recalled by Lyrical Foods Inc Due to Lyrical Foods...

The Issue: Lyrical Foods is voluntarily recalling four flavors of Kite Hill Almond...

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

Class II — Potential Health HazardOngoing
Refund
FoodJune 7, 2017· Lyrical Foods Inc

Recalled Item: Kite Hill Almond Yogurt Recalled by Lyrical Foods Inc Due to Lyrical Foods...

The Issue: Lyrical Foods is voluntarily recalling four flavors of Kite Hill Almond...

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

Class II — Potential Health HazardOngoing
Refund
FoodJune 7, 2017· Lyrical Foods Inc

Recalled Item: Kite Hill Almond Yogurt Recalled by Lyrical Foods Inc Due to Lyrical Foods...

The Issue: Lyrical Foods is voluntarily recalling four flavors of Kite Hill Almond...

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

Class II — Potential Health HazardOngoing
Refund
FoodJune 7, 2017· Lyrical Foods Inc

Recalled Item: Kite Hill Almond Yogurt Recalled by Lyrical Foods Inc Due to Lyrical Foods...

The Issue: Lyrical Foods is voluntarily recalling four flavors of Kite Hill Almond...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJune 6, 2017· Microbiologics Inc

Recalled Item: Microbiologics QC Sets and Panels. BD MAX" CT/GC/TV Verification and...

The Issue: Real-time shelf life testing failed at 24 months

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 6, 2017· Microbiologics Inc

Recalled Item: Microbiologics QC Sets and Panels: Helix Elite. Extended Enteric Bacterial...

The Issue: Real-time shelf life testing failed at 24 months

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 6, 2017· Microbiologics Inc

Recalled Item: Helix Elite" Molecular Standards: Inactivated Standard. Inactivated...

The Issue: Real-time shelf life testing failed at 24 months

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 6, 2017· Microbiologics Inc

Recalled Item: Helix Elite" Molecular Standards: Inactivated Standard. Inactivated...

The Issue: Real-time shelf life testing failed at 24 months

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 6, 2017· Microbiologics Inc

Recalled Item: Helix Elite" Molecular Standards: Inactivated Standard. Inactivated...

The Issue: Real-time shelf life testing failed at 24 months

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

Class II — Potential Health HazardOngoing