Product Recalls in Oklahoma
Product recalls affecting Oklahoma — including food, drugs, consumer products, medical devices, and vehicles distributed to Oklahoma. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 1,070 recalls have been distributed to Oklahoma in the last 12 months.
Showing 15001–15020 of 28,654 recalls
Recalled Item: Naera Hospital Bassinet Recalled by Stryker Medical Division of Stryker...
The Issue: It was identified that the volume of air inside the mattress may expand in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips HeartStart FR3 Defibrillator Recalled by Philips Electronics North...
The Issue: Automated external defibrillators may not fully meet IPx5 water ingress...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Theragenics Applicator Needle (18g x 20cm) The device is comprised Recalled...
The Issue: Some of the pouches containing Brachytherapy Applicator Needles (18g x 20cm)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fresenius Granuflo Dry Acid Concentrate- 3K 2.5 Ca 1 Mg Recalled by...
The Issue: Discolored powder has confirmed the presence of a foreign substance
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fresenius Granuflo Dry Acid Concentrate- 2K 2.0 Ca 1 Mg Recalled by...
The Issue: Discolored powder has confirmed the presence of a foreign substance
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fresenius Granuflo Dry Acid Concentrate- 2K 2.5 Ca 1 Mg Recalled by...
The Issue: Discolored powder has confirmed the presence of a foreign substance
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BrightMatter Guide Recalled by Synaptive Medical Inc Due to This recall has...
The Issue: This recall has been initiated due to a software defect found in the Guide...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS¿ Chemistry Products dLDL Reagent-GENs 26 & 27. In Vitro Recalled by...
The Issue: VITROS Chemistry Products dLDL Reagent GENs 26 and 27, negatively biased results
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Spirit Plus Bed Recalled by Stryker Medical Division of Stryker...
The Issue: The beds with the high rail side rail option may not be complaint with IEC...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Spirit Select Bed Recalled by Stryker Medical Division of Stryker...
The Issue: The beds with the high rail side rail option may not be complaint with IEC...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Thermoset Room Temperature Closed Loop Injectate Delivery System. 1 unit...
The Issue: Potential for leakage due to defect in the thermoset check valve component.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Giraffe Omnibed - Product Usage: The OmniBed is a combination Recalled by...
The Issue: GE Healthcare has become aware of a potential safety issue that can occur if...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Iced Thermoset Closed-Loop Injectate Delivery System for cold Injectate. 1...
The Issue: Potential for leakage due to defect in the thermoset check valve component.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Iced Thermoset Closed-Loop Injectate Delivery System for cold Injectate. 1...
The Issue: Potential for leakage due to defect in the thermoset check valve component.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hemoglobin A1c Control Recalled by Tosoh Bioscience Inc Due to Tosoh...
The Issue: Tosoh Bioscience has become aware of potential degradation of HbA1c control...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE HEALTHCARE CARESCAPE R860 Inspiratory Safety Guard Recalled by GE...
The Issue: The ventilator Inspiratory Safety Guard (ISG) may disconnect from the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AIA-900 Automated Immunoassay Analyzer Recalled by Tosoh Bioscience Inc Due...
The Issue: Tosoh Bioscience has become aware of a potential issue with the axis base of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Parietex Composite Parastomal Mesh (Product Number PCOPM15 / PCOPM20)...
The Issue: The firm is issuing this voluntary removal following receipt of reports of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AIA-900 Analyzer Recalled by Tosoh Bioscience Inc Due to Tosoh Bioscience...
The Issue: Tosoh Bioscience has become aware of a potential issue with the pickup arm...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SIGNA Architect system Product Usage: The Signa Architect system is Recalled...
The Issue: A small area on the bore surface, which is normally accessible to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.