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. 2,411 recalls have been distributed to Mississippi in the last 12 months.
Showing 41321–41340 of 49,744 recalls
Recalled Item: GE Healthcare Recalled by GE Healthcare, LLC Due to Possible sound loss...
The Issue: Possible sound loss associated with the CARESCAPE Monitor B650. When an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: H4051 Endo Tube Holder Recalled by Smiths Medical ASD, Inc. Due to The tube...
The Issue: The tube fastener on the ET Tube Holder may compress the tracheal tube when...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: H4002S Neonatal/Paed.Intubation Kit 3.0mm Murphy Recalled by Smiths Medical...
The Issue: The tube fastener on the ET Tube Holder may compress the tracheal tube when...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: H4052 Endo Tube Holder Recalled by Smiths Medical ASD, Inc. Due to The tube...
The Issue: The tube fastener on the ET Tube Holder may compress the tracheal tube when...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: H4002PS Neonatal/Paed.Intubation Kit 3.0mm Murphy Recalled by Smiths Medical...
The Issue: The tube fastener on the ET Tube Holder may compress the tracheal tube when...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 4001PS Neonatal/Paed.Intubation Kit 2.5mm Murphy Recalled by Smiths Medical...
The Issue: The tube fastener on the ET Tube Holder may compress the tracheal tube when...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: H4001S Neonatal/Paed.Intubation Kit 2.5mm Murphy Recalled by Smiths Medical...
The Issue: The tube fastener on the ET Tube Holder may compress the tracheal tube when...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS 4600 Chemistry System (VITROS 5 Recalled by Ortho-Clinical...
The Issue: Ortho Clinical Diagnostics has identified an anomaly with VITROS System...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS 3600 Immunodiagnostic System --- For use in the in vitro quantitative...
The Issue: Ortho Clinical Diagnostics has identified an anomaly with VITROS System...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS 5600 Integrated System --- For use in the in vitro quantitative...
The Issue: Ortho Clinical Diagnostics has identified an anomaly with VITROS System...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Excella II Standard Pedicle Screw Recalled by Innovasis, Inc Due to Mislabeling
The Issue: Innovasis is recalling the Excella II Standard Pedicle Screw due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Metoprolol Succinate Extended-release Tablets Recalled by Mylan...
The Issue: Presence of Foreign Tablets/Capsules: A pharmacist reported a rogue tablet...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Triamcinolone Acetonide Lotion USP Recalled by Fougera Pharmaceuticals Inc....
The Issue: Failed PH Specifications: It has been determined that the pH of the lots...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Diltiazem HCl Extended-release Capsules Recalled by Mylan Institutional,...
The Issue: Failed Impurities/Degradation Specifications: High out-of-specification...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Triamcinolone Acetonide Lotion USP Recalled by Fougera Pharmaceuticals Inc....
The Issue: Failed PH Specifications: It has been determined that the pH of the lots...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: UltraBalance Protein Powder Recalled by Metagenics, Inc. Due to Undeclared Soy
The Issue: Metagenics is recalling UltraBalance Protein powder because it may contain...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: CooperSurgical H/S CATHETER (PART # 61-5007) Intended for Hysterosonography/...
The Issue: Unsealed pouches.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IntelePACS software versions 3-8-1 to 4-9-1 Recalled by Intelerad Medical...
The Issue: In specific situation a partially truncated file may be written to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: E-Z-HD (barium sulfate) For Suspension (98% w/w) Recalled by Bracco...
The Issue: Subpotent Drug: Low out of specification results for both pH and assay...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: The Plum A+ Infusion System is designed to meet the Recalled by Hospira Inc....
The Issue: One lot of alarm assemblies used in Plum A+ and Plum A+3 infusion pumps may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.