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. 2,641 recalls have been distributed to Oregon in the last 12 months.

50,914 total recalls
2,641 in last 12 months

Showing 81818200 of 28,488 recalls

Medical DeviceApril 7, 2022· MALVERN PANALYTICAL LTD

Recalled Item: NanoSight NS300 Recalled by MALVERN PANALYTICAL LTD Due to Product found to...

The Issue: Product found to not comply to Class 1 Laser safety requirement.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 7, 2022· Bio-Rad Laboratories, Inc.

Recalled Item: Resin UPDATE CD-ROM Recalled by Bio-Rad Laboratories, Inc. Due to The...

The Issue: The problem is with the Bio-Rad VARIANT nbs Sickle Cell Program Resin Update...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 7, 2022· Synthes (USA) Products LLC

Recalled Item: Radial Head Replacement System Implant is a one-piece Recalled by Synthes...

The Issue: DePuy Synthes Radial Head Replacement System Contraindications added to...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 6, 2022· MESA BIOTECH, INC

Recalled Item: Accula SARS-CoV-2 Test Recalled by MESA BIOTECH, INC Due to SARS-CoV-2 Test...

The Issue: SARS-CoV-2 Test has an increased potential for false positive results, which...

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 6, 2022· Johnson & Johnson Surgical Vision Inc

Recalled Item: TRAY RING COVER Recalled by Johnson & Johnson Surgical Vision Inc Due to...

The Issue: Potential breach in the sterility barrier for tray ring covers.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 5, 2022· ARJOHUNTLEIGH POLSKA Sp. z.o.o.

Recalled Item: Sara Plus Active Floor Lift Recalled by ARJOHUNTLEIGH POLSKA Sp. z.o.o. Due...

The Issue: The device may emit smoke or ignite.

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

Class I — Serious Health HazardOngoing
Medical DeviceApril 5, 2022· Certified Safety Mfg Inc

Recalled Item: The following first aid kits and cabinets containing components Medi-First...

The Issue: First aid kit and cabinet components are being recalled by the supplier due...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 4, 2022· USA Medical, LLC

Recalled Item: Diagnostic Kit SARS-cCo V Antigen Rapid Test Recalled by USA Medical, LLC...

The Issue: COVID-19/SARS-CoV-2 Antigen Tests did not receive FDA Emergency Use...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 1, 2022· Karl Storz Endoscopy

Recalled Item: 11272V CMOS VIDEO-CYSTO-URETHROSCOPE REV 11272VA 11272VAK CMOS...

The Issue: Failure to achieve the expected six-log reduction in microorganisms...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 1, 2022· Karl Storz Endoscopy

Recalled Item: 11278VSA 11278VSAK Flexible Video-Uretero-Renoscope (FLEX-XC) Z23117US-BA...

The Issue: Failure to achieve the expected six-log reduction in microorganisms...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 1, 2022· CooperSurgical, Inc.

Recalled Item: VITRIGUARD Recalled by CooperSurgical, Inc. Due to Products in this lot may...

The Issue: Products in this lot may have compromised barrier seals, introducing a risk...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 1, 2022· Karl Storz Endoscopy

Recalled Item: 11005BC1 11005BCK1 Flexible Bronchoscope Z21493US-BA (06/2019) Recalled by...

The Issue: Failure to achieve the expected six-log reduction in microorganisms...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 1, 2022· Karl Storz Endoscopy

Recalled Item: 11278A2 11278AK2 Flexible Ureteroscope Z20615US-BA (08-2018) Recalled by...

The Issue: Failure to achieve the expected six-log reduction in microorganisms...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 1, 2022· Karl Storz Endoscopy

Recalled Item: CYSTO-URETHRO-FIBERSCOPE CYSTOSCOPE Recalled by Karl Storz Endoscopy Due to...

The Issue: Failure to achieve the expected six-log reduction in microorganisms...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 1, 2022· Karl Storz Endoscopy

Recalled Item: 11272VH-TL 11272VHK-TL HD-VIEW Flexible HD Cysto-Urethroscope Z23875US-BC...

The Issue: Failure to achieve the expected six-log reduction in microorganisms...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 1, 2022· Karl Storz Endoscopy

Recalled Item: 11278VSA 11278VSAK Flexible Video-Uretero-Renoscope (FLEX-XC) Z23117US-BA...

The Issue: Failure to achieve the expected six-log reduction in microorganisms...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 1, 2022· Karl Storz Endoscopy

Recalled Item: 11274BCU1 11274BCUK1 Flexible Cystoscope Z18449US-BD (08-2018) Recalled by...

The Issue: Failure to achieve the expected six-log reduction in microorganisms...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 1, 2022· Karl Storz Endoscopy

Recalled Item: 11272VUE 11272VUEK Flexible Video Cysto-Urethroscope 96136031USCA V1.1...

The Issue: Failure to achieve the expected six-log reduction in microorganisms...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 1, 2022· Karl Storz Endoscopy

Recalled Item: 11001RD1 11001RDK1 KARL STORZ Slim Nasopharyngolaryngoscope 96216006US V5.0...

The Issue: Failure to achieve the expected six-log reduction in microorganisms...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 1, 2022· Karl Storz Endoscopy

Recalled Item: 11272VN 11272VNK Flexible Video Urethro Cystoscope Z18442US-BD (08/2018)...

The Issue: Failure to achieve the expected six-log reduction in microorganisms...

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

Class II — Potential Health HazardOngoing