Product Recalls in Wyoming
Product recalls affecting Wyoming — including food, drugs, consumer products, medical devices, and vehicles distributed to Wyoming. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,503 recalls have been distributed to Wyoming in the last 12 months.
Showing 14541–14560 of 27,462 recalls
Recalled Item: Zimmer Compress Devices and Instruments: Item Number/Item Description 178350...
The Issue: Correction to update the surgical technique for the Compress System. To make...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARCHITECT Free T3 Reagent Kit used on ARCHITECT i1000SR or Recalled by...
The Issue: Samples tested using ARCHITECT Free T3 or ARCHITECT Total T3 assays may show...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atrium 28Fr PVC Thoracic Catheter RIGHT ANGLE Recalled by Atrium Medical...
The Issue: This recall has been initiated in response to a seal defect found in certain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: St. Jude Medical InfinityTM DBS System 8CH Directional Lead Recalled by St....
The Issue: The most proximal unsegmented electrode of the Deep Brain Stimulation leads,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dimension Vista Lactate Dehydrogenase (LDI) Flex reagent cartridge Recalled...
The Issue: Siemens Healthcare Diagnostics has confirmed that Dimension Vista Lactate...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
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: IntelliVue MX40 Patient Monitor Recalled by Philips Electronics North...
The Issue: A problem has been detected in the Philips IntelliVue MX4O that, if it were...
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: 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: 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- 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: 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- 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: 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: 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: 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: 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: 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: 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.