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. 2,466 recalls have been distributed to Wyoming in the last 12 months.
Showing 16041–16060 of 48,219 recalls
Recalled Item: A calculator/data processing module for clinical use is an electronic...
The Issue: A software error results in the unintentional removal of the serum-indices...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EXOGEN Ultrasound Coupling Gel Recalled by Bioventus, LLC Due to Product may...
The Issue: Product may contain white particulates that are microbial in nature.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Succinylcholine Chloride PF Inj. 200 mg/10 mL Recalled by US Compounding Inc...
The Issue: Labeling: Incorrect or Missing lot and/or expiration date: The lot number...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: KWIK-STI(TM) Recalled by Microbiologics Inc Due to The expiration date on...
The Issue: The expiration date on the label of one component (negative control 0243U)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: X1 Recalled by Medtronic Neurosurgery Due to Neonatal Valves were...
The Issue: Neonatal Valves were manufactured with a ventricular catheter connection...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: X1 Recalled by Medtronic Neurosurgery Due to Neonatal Valves were...
The Issue: Neonatal Valves were manufactured with a ventricular catheter connection...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: X1 Recalled by Medtronic Neurosurgery Due to Neonatal Valves were...
The Issue: Neonatal Valves were manufactured with a ventricular catheter connection...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Disposable Humidification Flask Recalled by Cook Medical Llc Due to A small...
The Issue: A small percentage of the Disposable Humidification Flasks may have a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: WAHL 4212 HEATED MASSAGER Recalled by Wahl Clipper Corp Due to The...
The Issue: The connection between the massager and heat element can overheat causing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Penumbra JET 7 KIT Reperfusion Catheter+Penumbra Hi-Flow Aspiration Tubing...
The Issue: The catheter may become susceptible to distal tip damage during use. Distal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Penumbra JET 7 Reperfusion Catheter The Penumbra JET Recalled by Penumbra...
The Issue: The catheter may become susceptible to distal tip damage during use. Distal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Penumbra JET 7MAX KIT Penumbra JET 7 Reperfusion Catheter+ MAX Recalled by...
The Issue: The catheter may become susceptible to distal tip damage during use. Distal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ACUITY Universal Cutter Recalled by Boston Scientific Corporation Due to...
The Issue: Boston Scientific (BSC) is retrieving five Model 7060 ACUITY cutters...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Penumbra JET 7 KIT Reperfusion Catheter+Penumbra Hi-Flow Aspiration Tubing...
The Issue: The catheter may become susceptible to distal tip damage during use. Distal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS XT Chemistry Products ALB-TP Slides (ALB is not affected) Recalled by...
The Issue: Eltrombopag Interference for VITROS Chemistry Products TP Slides and VITROS...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS Chemistry Products TP Slides- IVD measure total protein (TP) Recalled...
The Issue: Eltrombopag Interference for VITROS Chemistry Products TP Slides and VITROS...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pinnacle Cups Recalled by DePuy Orthopaedics, Inc. Due to Certain Pinnacle...
The Issue: Certain Pinnacle Cup devices may potentially exhibit an oversized "minor...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PORTEX Bivona Cuffless Neonatal/Pediatric FlexTend Tracheostomy Tube...
The Issue: A specific model and lot number of Bivona Cuffless FlexTend Tracheostomy...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vasopressin 20 Units added to 0.9% Sodium Chloride 100 mL Rx Only Recalled...
The Issue: Subpotent drug.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Azacitidine for Injection 100 mg/vial For Subcutaneous and Intravenous Use...
The Issue: cGMP deviations: Vials may not be sealed correctly affecting sterility.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.