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. 2,457 recalls have been distributed to Oregon in the last 12 months.
Showing 27101–27120 of 28,488 recalls
Recalled Item: DePuy Spine VIPER POLY SCREW 5.5 8 X70MM Tl Product Recalled by DePuy Spine,...
The Issue: Polyaxial screws 8x 80 and larger may disassociate when inserting in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DePuy Spine VIPER POLY SCREW 5.5 10X100MM Tl Product Code: Recalled by DePuy...
The Issue: Polyaxial screws 8x 80 and larger may disassociate when inserting in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DePuy Spine VIPER POLY SCREW 5.5 9 X 80MM Tl Recalled by DePuy Spine, Inc....
The Issue: Polyaxial screws 8x 80 and larger may disassociate when inserting in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DePuy Spine VIPER POLY SCREW 5.5 10 X 80MM Tl Recalled by DePuy Spine, Inc....
The Issue: Polyaxial screws 8x 80 and larger may disassociate when inserting in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 25-Hydroxy Vitamin D EIA Recalled by IDS (Immunodiagnostic Systems Ltd.) Due...
The Issue: Immunodiagnostic Systems is recalling the 25-Hydroxy Vitamin D EIA, AC-57F1...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DePuy Spine VIPER POLY SCREW 5.5 8 X80MM Tl Product Recalled by DePuy Spine,...
The Issue: Polyaxial screws 8x 80 and larger may disassociate when inserting in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Eterna Giovinezza System Recalled by Quanta System, S.p.A. Due to Quanta...
The Issue: Quanta System S.p.A, Italy, is notifying U.S. consignees that their website...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ultrawave II EX 1320/ Ultrawave III EX 1320 Powered Laser Recalled by Quanta...
The Issue: Quanta System S.p.A, Italy, is notifying U.S. consignees that their website...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Q-Plus T Powered Laser Surgical Instrument Nd:YAG 1064 nm and Recalled by...
The Issue: Quanta System S.p.A, Italy, is notifying U.S. consignees that their website...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Echo Bi-Metric Press-Fit Stems/Echo Bi-Metric 11mm x 135mm Collarless Porous...
The Issue: It was reported that the surgeon noticed that the Echo 11mm hip stem had an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Invacare Height Adjustable (walking) Canes Recalled by Invacare Corporation...
The Issue: Following their receipt of several customer complaints, Invacare recalled...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Phoenix PMIC-108 Panels Recalled by Becton Dickinson & Co. Due to An...
The Issue: An antibiotic susceptibility test kit may produce false intermediate or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ethicon Endo-Surgery Inc. The ENSEAL¿ G2 Tissue Sealers are indicated...
The Issue: Potential for self activation while the device is in use, which may result...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MAYFIELD Composite Series Base Unit Recalled by Integra LifeSciences...
The Issue: An investigation of an adverse trend of complaints conducted by Integra...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OmniGuide BP-ROBOTIC ( BeamPath Robotic) Recalled by OmniGuide, Inc. Due to...
The Issue: Failure of glue joint, allowed a portion of the single use device to shift...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arobella Medical 6mm Qurette used with the Arobella Medical AR1000 Recalled...
The Issue: This recall has been initiated because the Arobella Medical 6mm Qurette Q07...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MAYFIELD Composite Series Skull Clamps Recalled by Integra LifeSciences...
The Issue: An investigation of an adverse trend of complaints conducted by Integra...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Access hLH assay is a paramagnetic particle Recalled by Beckman Coulter...
The Issue: Beckman Coulter Inc. (BEC) has demonstrated that real time stability testing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lifestyles Pleasure Collection 30 Premium Lubricated Condoms Assortment of...
The Issue: One lot of Lifestyles Pleasure Collection Lubricated Condoms is misbranded....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Laparoscope Recalled by Applied Medical Resources Corp Due to Applied...
The Issue: Applied Medical is conducting a voluntary recall on a specific lot number of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.