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. 2,544 recalls have been distributed to Oregon in the last 12 months.
Showing 18361–18380 of 28,488 recalls
Recalled Item: VITEK¿ 2 Gram Negative Susceptibility card (AST-N211) Recalled by Biomerieux...
The Issue: The integrity of the product container may be compromised thereby exposing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITEK¿ 2 Gram Negative Susceptibility card (AST-N286) Recalled by Biomerieux...
The Issue: The integrity of the product container may be compromised thereby exposing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITEK¿ 2 Gram Negative Susceptibility card (AST-N363) Recalled by Biomerieux...
The Issue: The integrity of the product container may be compromised thereby exposing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITEK¿ 2 Gram Positive Susceptibility card (AST-GP67) Recalled by Biomerieux...
The Issue: The integrity of the product container may be compromised thereby exposing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITEK¿ 2 Gram Negative Susceptibility card (AST-GN76) Recalled by Biomerieux...
The Issue: The integrity of the product container may be compromised thereby exposing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITEK¿ 2 Gram Streptococcus Susceptibility card (AST-ST01) Recalled by...
The Issue: The integrity of the product container may be compromised thereby exposing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITEK¿ 2 Gram Positive Susceptibility card (AST-P605) Recalled by Biomerieux...
The Issue: The integrity of the product container may be compromised thereby exposing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITEK¿ 2 Gram Negative Susceptibility card (AST-N340) Recalled by Biomerieux...
The Issue: The integrity of the product container may be compromised thereby exposing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITEK¿ 2 Fungal Susceptibility card (AST-YS08) Recalled by Biomerieux Inc...
The Issue: The integrity of the product container may be compromised thereby exposing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITEK¿ 2 Gram Negative Susceptibility card (AST-N265) Recalled by Biomerieux...
The Issue: The integrity of the product container may be compromised thereby exposing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITEK¿ 2 Gram Negative Susceptibility card (AST-N203) Recalled by Biomerieux...
The Issue: The integrity of the product container may be compromised thereby exposing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITEK¿ 2 Gram Negative Susceptibility card (AST-N353) Recalled by Biomerieux...
The Issue: The integrity of the product container may be compromised thereby exposing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: High Frequency Resection Electrodes Recalled by Olympus Corporation of the...
The Issue: Loop wires breaking at the distal end of the Monopolar HF Resection Electrodes.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARCHITECT SHBG Reagent The ARCHITECT SHBG assay is a chemiluminescent...
The Issue: Firm has identified that ARCHITECT SHBG results generated with the Potassium...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AFFIXUS Hip Fracture Nail Product Usage: The Hip Fracture Nail Recalled by...
The Issue: nail not properly engaging with the targeting jig due to certain undersized...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CSI Recalled by Cardiovascular Systems Inc Due to Cardiovascular Systems,...
The Issue: Cardiovascular Systems, Inc. (CSI). has initiated a recall to remove 1,396...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 9200C and 9200D Laryngeal Strobe Product Usage: The 9310HD is Recalled by...
The Issue: Pentax Medical did not always provide transformers with 9175 isolation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CardioTek EP-TRACER Software V1.x and V2.0 The EP-TRACER System is Recalled...
The Issue: Software bug which allows parameters to be changed unintentionally during use.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 9400 Laryngeal Strobe Product Usage: The 9310HD is used to Recalled by...
The Issue: Pentax Medical did not always provide transformers with 9175 isolation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 7245C Recalled by Pentax of America Inc Due to Pentax Medical did not always...
The Issue: Pentax Medical did not always provide transformers with 9175 isolation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.