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. 2,646 recalls have been distributed to Oregon in the last 12 months.

50,914 total recalls
2,646 in last 12 months

Showing 65616580 of 28,488 recalls

Medical DeviceApril 17, 2023· Draeger Medical, Inc.

Recalled Item: Ventstar Coax Recalled by Draeger Medical, Inc. Due to Glued connections of...

The Issue: Glued connections of the breathing circuit can become loose before or during...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 17, 2023· Draeger Medical, Inc.

Recalled Item: ID Circuit Basic (P) 180 Recalled by Draeger Medical, Inc. Due to Glued...

The Issue: Glued connections of the breathing circuit can become loose before or during...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 17, 2023· Draeger Medical, Inc.

Recalled Item: VentStar Basic (P)250 Recalled by Draeger Medical, Inc. Due to Glued...

The Issue: Glued connections of the breathing circuit can become loose before or during...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 17, 2023· Draeger Medical, Inc.

Recalled Item: Anesthesia Circuit Kit Coax 3 Recalled by Draeger Medical, Inc. Due to Glued...

The Issue: Glued connections of the breathing circuit can become loose before or during...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 17, 2023· Draeger Medical, Inc.

Recalled Item: Ventstar Coax 180 Recalled by Draeger Medical, Inc. Due to Glued connections...

The Issue: Glued connections of the breathing circuit can become loose before or during...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 17, 2023· Draeger Medical, Inc.

Recalled Item: Anesthesia Circuit Kit Coax 1 Recalled by Draeger Medical, Inc. Due to Glued...

The Issue: Glued connections of the breathing circuit can become loose before or during...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 17, 2023· Draeger Medical, Inc.

Recalled Item: VentStar Basic (N) 180 Recalled by Draeger Medical, Inc. Due to Glued...

The Issue: Glued connections of the breathing circuit can become loose before or during...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 17, 2023· Draeger Medical, Inc.

Recalled Item: VentStar breathing bag Set (P) 110 Recalled by Draeger Medical, Inc. Due to...

The Issue: Glued connections of the breathing circuit can become loose before or during...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 17, 2023· Draeger Medical, Inc.

Recalled Item: Anesthesia Circuit Kit Coax HEPA Recalled by Draeger Medical, Inc. Due to...

The Issue: Glued connections of the breathing circuit can become loose before or during...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 17, 2023· Draeger Medical, Inc.

Recalled Item: Ventstar Coax 230 Recalled by Draeger Medical, Inc. Due to Glued connections...

The Issue: Glued connections of the breathing circuit can become loose before or during...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 17, 2023· Draeger Medical, Inc.

Recalled Item: VentStar Bag Set (N) 110 Recalled by Draeger Medical, Inc. Due to Glued...

The Issue: Glued connections of the breathing circuit can become loose before or during...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 17, 2023· Draeger Medical, Inc.

Recalled Item: VentStar Watertrap (P) 180 w/oLL Recalled by Draeger Medical, Inc. Due to...

The Issue: Glued connections of the breathing circuit can become loose before or during...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 17, 2023· Draeger Medical, Inc.

Recalled Item: VentStar Coax (P) 150 Recalled by Draeger Medical, Inc. Due to Glued...

The Issue: Glued connections of the breathing circuit can become loose before or during...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 17, 2023· Draeger Medical, Inc.

Recalled Item: ID Coax 180 Recalled by Draeger Medical, Inc. Due to Glued connections of...

The Issue: Glued connections of the breathing circuit can become loose before or during...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 14, 2023· Mechatronics USA

Recalled Item: RR Mechatronics Starrsed Control Level N ESR Control 4.6 ml Recalled by...

The Issue: QRR049001 Lot QCAB6AN505 incorrectly labelled as QRR049002 Lot QCAB6AAA28....

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

Class III — Low RiskOngoing
Medical DeviceApril 14, 2023· Mechatronics USA

Recalled Item: RR Mechatronics Control Level A ESR Control4.6 ml QRR049002- In-vitro...

The Issue: QRR049001 Lot QCAB6AN505 incorrectly labelled as QRR049002 Lot QCAB6AAA28....

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

Class III — Low RiskOngoing
Medical DeviceApril 14, 2023· Ortho-Clinical Diagnostics, Inc.

Recalled Item: VITROS Chemistry Products Calibrator Kit 11 VANC Reagent Generation (GEN)...

The Issue: Unavailable to calibrate VITROS Chemistry Products VANC Reagent, Generation...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 13, 2023· DePuy Mitek, Inc., a Johnson & Johnson Co.

Recalled Item: DePuy Mitek BIOKNOTLESS Plus w/ Panacryl-Indicated for use in soft Recalled...

The Issue: IFU Warning: Applying bending force and/or bending force with impaction to...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 13, 2023· DePuy Mitek, Inc., a Johnson & Johnson Co.

Recalled Item: DePuy Mitek BIOKNOTLESS Plus w/ OC-Indicated for use in soft Recalled by...

The Issue: IFU Warning: Applying bending force and/or bending force with impaction to...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 13, 2023· DePuy Mitek, Inc., a Johnson & Johnson Co.

Recalled Item: DePuy Mitek BIOKNOTLESS Rapid W/ OC-Indicated for use in soft Recalled by...

The Issue: IFU Warning: Applying bending force and/or bending force with impaction to...

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

Class II — Potential Health HazardOngoing