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. 2,448 recalls have been distributed to Wyoming in the last 12 months.
Showing 18261–18280 of 48,219 recalls
Recalled Item: Fresenius 2008T Hemodialysis Machine: Part Number Description 190573 2008T...
The Issue: A "Remove USB Device 2" false alarm may be displayed when no USB device or a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fresenius 2008T BlueStar Hemodialysis Machine Part Number Description:...
The Issue: A "Remove USB Device 2" false alarm may be displayed when no USB device or a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VACUETTE Tube 2ml 9NC Coagulation Sodium Citrate 3.2%. Item no. Recalled by...
The Issue: Concerned lot of VACETTE 2mL 9NC Coagulation Tubes were shown to have...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pantoprazole Sodium Delayed-Release Tablets Recalled by Jubilant Cadista...
The Issue: CGMP Deviations: Presence of dark brown discoloration on edges of tablets
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Endocuff Vision: models ARV 110 Recalled by Boddingtons Plastics Ltd Due to...
The Issue: Updated Instructions For Use- to contraindications and potential...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SkyVision SDS System - Video Integration Model: GC-SDS-BSCB-200 - Product...
The Issue: Intermittent failure of a signal being sent to a monitor from the touch...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ACMI 9FR PROBE (E4-9F) Manufactured for Olympus Surgical Technologies...
The Issue: Investigation into a biocompatibility test discrepancy where a lot failed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Probe Recalled by Northgate Technologies, Inc. Due to As part of an...
The Issue: As part of an investigation into a biocompatibility test discrepancy where a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AUTOLITH URO-TCH 9FR PROBE 54CM Recalled by Northgate Technologies, Inc. Due...
The Issue: Investigation into a biocompatibility test discrepancy where a lot failed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS Immunodiagnostic Products TT4 Reagent Pack Recalled by Ortho Clinical...
The Issue: The specified reagent packs exhibit an increase in the frequency of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ABL800 FLEX Recalled by Radiometer Medical ApS Due to Analyzer's barcode...
The Issue: Analyzer's barcode reader misinterprets the contents of barcode label used...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sotalol HCL Tablets Recalled by Mylan Pharmaceuticals Inc. Due to Presence...
The Issue: Presence of particulate matter. presence of metal particles.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Atorvastatin Calcium Tablets Recalled by Sun Pharmaceutical Industries, Inc....
The Issue: Presence of foreign substance: Foreign matter has been identified as latex...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Levonorgestrel and Ethinyl Estradiol Tablets USP Recalled by Lupin...
The Issue: Failed Content Uniformity Specifications: Out Of Specification test results...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Bekyree (desogestrel and ethinyl estradiol tablets USP Recalled by Lupin...
The Issue: Failed Content Uniformity Specifications: Out Of Specification test results...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Custom convenience kits containing Medline brand Sterile Pre-Saturated...
The Issue: Medline identified that there may be a potential for voids in the packaging...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Percuflex Plus Ureteral Stent Set 6FX26CM with .038 Sensor UPN:...
The Issue: An increase in the rate of complaints for difficulty or inability to track...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Polaris Ultra Ureteral Stent Set 6FX24CM with .035 Sensor UPN: M006192132080...
The Issue: An increase in the rate of complaints for difficulty or inability to track...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sensor Nitinol Wire with Hydrophilic Tip .0383CM FLEX ANG/150CM UPN:...
The Issue: An increase in the rate of complaints for difficulty or inability to track...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sensor Nitinol Wire with Hydrophilic Tip .035 3CM FLEX /150CM Recalled by...
The Issue: An increase in the rate of complaints for difficulty or inability to track...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.