Product Recalls in Mississippi
Product recalls affecting Mississippi — including food, drugs, consumer products, medical devices, and vehicles distributed to Mississippi. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 1,744 recalls have been distributed to Mississippi in the last 12 months.
Showing 42841–42860 of 49,744 recalls
Recalled Item: Rusch Brochopart and Rusch Brochopart White The Rush Endobronchial Tube...
The Issue: The product may fail to achieve seal of right lung due to the cuff inflating...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Model EPIQ 5 Ultrasound System. Intended for diagnostic ultrasound...
The Issue: A problem has been detected with Philips Model EPIQ 5 and 7 Ultrasound...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Model EPIQ 7 Ultrasound System. Intended for diagnostic ultrasound...
The Issue: A problem has been detected with Philips Model EPIQ 5 and 7 Ultrasound...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Popsicle Orange Cherry Grape 20 pops Net 33 fl oz Unilever Englewood Cliffs...
The Issue: Unilever United States, Inc. is voluntarily recalling a limited number of...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Medtronic neurostimulators. Restore (37711) Recalled by Medtronic...
The Issue: Medtronic neurostimulators (used with pain and deep brain stimulation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Recalled by Medtronic Neuromodulation Due to Medtronic...
The Issue: Medtronic neurostimulators (used with pain and deep brain stimulation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: D-10" Hemoglobin Testing System Recalled by Bio-Rad Laboratories, Inc. Due...
The Issue: On a rare occasion the D-10 software might generate an extra result by...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PowerPort Slim Implantable Port Recalled by Bard Access Systems Due to...
The Issue: Labeling discrepancy.The label states that the implantable port contains...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic Activa RC (37612) Recalled by Medtronic Neuromodulation Due to...
The Issue: Medtronic neurostimulators (used with pain and deep brain stimulation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Novocastra Liquid Mouse Monoclonal Antibody Glutathione S-Transferase pi...
The Issue: Novocastra Liquid Mouse Monoclonal Antibody Glutathione S-Transferase pi...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Advil PM Caplets Recalled by Pfizer Us Pharmaceutical Group Due to Subpotent...
The Issue: Subpotent Drug: This lot is being recalled because of out-of-specification...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Part 475625 Recalled by Biomet, Inc. Due to Incorrect labeling on specific...
The Issue: Incorrect labeling on specific lots of the Intramedullary Bone Saw. The Saw...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Part 475620 Intramedullary Bone Saw CAM Assembly Size 12mm Recalled by...
The Issue: Incorrect labeling on specific lots of the Intramedullary Bone Saw.The Saw...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Part 475630 Recalled by Biomet, Inc. Due to Incorrect labeling on specific...
The Issue: Incorrect labeling on specific lots of the Intramedullary Bone Saw. The Saw...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Natural-Knee¿ II - Unicompartmental Knee Prosthesis: CONG TIB INS SZ1/2...
The Issue: A complaint was received for a discolored All Poly Tibia. Root cause...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Apollo Knee Tibial Baseplate/Knee Tibial Insert: CONG TIB INS SZ0/19MM...
The Issue: A complaint was received for a discolored All Poly Tibia. Root cause...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Natural-Knee¿ N-K II DOMED ALL-POLY PAT Recalled by Zimmer, Inc. Due to A...
The Issue: A complaint was received for a discolored All Poly Tibia. Root cause...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MOST Options" System (MOST) HINGED TIB INS SZ 1 16MM Recalled by Zimmer,...
The Issue: A complaint was received for a discolored All Poly Tibia. Root cause...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Natural-Knee¿ Congruent Tibial Insert with Screw: SF-CON TIB INS LT Recalled...
The Issue: A complaint was received for a discolored All Poly Tibia. Root cause...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Natural-Knee¿ II Posterior Stabilized (P.S.) Condylar Tibial Inserts: N-K II...
The Issue: A complaint was received for a discolored All Poly Tibia. Root cause...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.