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. 2,557 recalls have been distributed to Oregon in the last 12 months.
Showing 17401–17420 of 28,488 recalls
Recalled Item: A.T.S. 4000TS Tourniquet Systems Recalled by Zimmer Surgical Inc Due to...
The Issue: Updated on-device label and 3 pages of an updated Operator/Service Manual....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VCLAS (Visualase Cooled Laser Ablation System) Part Number: 9735559...
The Issue: The VCLAS 3mm, 10mm, and 15mm tip devices were not appropriately tested for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: A.T.S. 2200TS Tourniquet Systems Recalled by Zimmer Surgical Inc Due to...
The Issue: Updated on-device label and 3 pages of an updated Operator/Service Manual....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: iFusion Recalled by Optovue, Inc. Due to FDA determined that a 510(k) is...
The Issue: FDA determined that a 510(k) is needed for the Vault Mapping software (also...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Concorde Lift Torque Limiting Handle. Must be used with supplemental...
The Issue: Potential for Intra-operative breakage of driver tips
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 2.5 mm Guide Rod Recalled by Synthes (USA) Products LLC Due to Possible lack...
The Issue: Possible lack of product sterility due to potential gaps/channeling in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 2.5 mm Reaming Rod Recalled by Synthes (USA) Products LLC Due to Possible...
The Issue: Possible lack of product sterility due to potential gaps/channeling in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Light Clip for Oracle Retractor Recalled by Synthes (USA) Products LLC Due...
The Issue: Possible lack of product sterility due to potential gaps/channeling in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 2.5 mm Reaming Rod Recalled by Synthes (USA) Products LLC Due to Possible...
The Issue: Possible lack of product sterility due to potential gaps/channeling in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 2.5 mm Reaming Rod Recalled by Synthes (USA) Products LLC Due to Possible...
The Issue: Possible lack of product sterility due to potential gaps/channeling in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 3.0 mm Reaming Rod Recalled by Synthes (USA) Products LLC Due to Possible...
The Issue: Possible lack of product sterility due to potential gaps/channeling in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 2.5 mm Titanium Calibrated Reaming Rod Recalled by Synthes (USA) Products...
The Issue: Possible lack of product sterility due to potential gaps/channeling in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Concorde Lift Driver Shaft AO. Used with supplemental internal spinal...
The Issue: Potential for Intra-operative breakage of driver tips
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Syngo Imaging version V31 (model # 10014063) is a Picture Recalled by...
The Issue: Siemens is releasing a letter to inform about potential data loss relevant...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ArrowADVANTAGE 5 Pressure Injectable Peripherally Inserted Central Catheter...
The Issue: Finished good kits may contain incorrect components. Kits that should...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARROW PICC powered by ARROW VPS Stylet Recalled by Arrow International Inc...
The Issue: Finished good kits may contain incorrect components. Kits that should...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: smith&nephew POLARSTEM(TM) Femoral Stems with Ti/HA (Standard Recalled by...
The Issue: The Cardan joint of the Polarstem Cardan could potentially fracture or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TUOHY Epidural Needle Recalled by Epimed International Due to Potential for...
The Issue: Potential for partially incomplete seal of product, impacting sterility.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Platinium VR 1210 Recalled by Sorin Group Italia SRL - CRF Due to There is a...
The Issue: There is a possibility of overconsumption of certain PLATINIUM Implantable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Platinium DR DF4 1540 Recalled by Sorin Group Italia SRL - CRF Due to There...
The Issue: There is a possibility of overconsumption of certain PLATINIUM Implantable...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.