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. 1,677 recalls have been distributed to Wyoming in the last 12 months.
Showing 43941–43960 of 48,219 recalls
Recalled Item: Brand Name: Multirate Infusor Devices. Indicated for the intravenous...
The Issue: Baxter Healthcare Corporation (Baxter) is issuing an Urgent Product Recall...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: SV Elastomeric Infusion Device. Indicated for the intravenous...
The Issue: Baxter Healthcare Corporation (Baxter) is issuing an Urgent Product Recall...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Coiled Tube Infusors (Portable Elastomeric Infusion Systems)....
The Issue: Due to an increase in complaints for leaks at the distal male Luer and Luer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Intermate Infusion Pump. Indicated for the intravenous...
The Issue: Baxter Healthcare Corporation (Baxter) is issuing an Urgent Product Recall...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Regional Analgesia Infusor System with Patient Control....
The Issue: Baxter Healthcare Corporation (Baxter) is issuing an Urgent Product Recall...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Intermate Infusion Pump. Indicated for the intravenous...
The Issue: Baxter Healthcare Corporation (Baxter) is issuing an Urgent Product Recall...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MedStream Programmable Infusion Pump- Implantable for the intrathecal...
The Issue: Miscalibrated Fill Level Sensor may affect dosing level
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 00597001101 Femur CR PRECOAT FEM COMP SIZE AML Recalled by Zimmer, Inc. Due...
The Issue: Surgeons are implanting components of the NexGen Cruciate Retaining (CR)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MedStream Programmable Infusion Pump Recalled by Codman & Shurtleff, Inc....
The Issue: Miscalibrated Fill Level Sensor may affect dosing level
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: vega one Recalled by Sequel Naturals Ltd Due to Raw material supplier of the...
The Issue: Raw material supplier of the chocolate used for the bar coating had milk...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: vega sport Recalled by Sequel Naturals Ltd Due to Raw material supplier of...
The Issue: Raw material supplier of the chocolate used for the bar coating had milk...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: vega one Recalled by Sequel Naturals Ltd Due to Raw material supplier of the...
The Issue: Raw material supplier of the chocolate used for the bar coating had milk...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: vega one Recalled by Sequel Naturals Ltd Due to Raw material supplier of the...
The Issue: Raw material supplier of the chocolate used for the bar coating had milk...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: vega sport Recalled by Sequel Naturals Ltd Due to Raw material supplier of...
The Issue: Raw material supplier of the chocolate used for the bar coating had milk...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: 00597504110 Provisional AC ART SURF PROV 56/STR GRN 10 Recalled by Zimmer,...
The Issue: Surgeons are implanting components of the NexGen Cruciate Retaining (CR)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 00597201333 Femur CR POR SURF HDN FEM CO-NID CML Recalled by Zimmer, Inc....
The Issue: Surgeons are implanting components of the NexGen Cruciate Retaining (CR)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 00597104110 Provisional CR ART SURF PROV 56/STR GRN 10 Recalled by Zimmer,...
The Issue: Surgeons are implanting components of the NexGen Cruciate Retaining (CR)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 00595203110 Articular Surface XLPE CR ART SURF 3 Recalled by Zimmer, Inc....
The Issue: Surgeons are implanting components of the NexGen Cruciate Retaining (CR)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 00595601201 Femur CR-FLEX OPT FEM B-L Rx Sterile Recalled by Zimmer, Inc....
The Issue: Surgeons are implanting components of the NexGen Cruciate Retaining (CR)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 00597203109 Articular Surface CR ART SURF 34/STRIPE YEL 09 Recalled by...
The Issue: Surgeons are implanting components of the NexGen Cruciate Retaining (CR)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.