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. 2,590 recalls have been distributed to Mississippi in the last 12 months.
Showing 15121–15140 of 28,172 recalls
Recalled Item: MOSAIQ Oncology Information System Recalled by Elekta, Inc. Due to Order...
The Issue: Order Status Remains Approved When Should Indicate Complete.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Palcam Agar Base Recalled by Acumedia Manufacturers, Inc. Due to Expiration...
The Issue: Expiration date on the label is incorrect. Correct expiration date was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vanguard 360 Revision Knee System 63x 10mm Universal Tibial Block Augment...
The Issue: The implant only has one bolt in the sterile package but it should have had two.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vanguard 360 Revision Knee System 75x 5mm Universal Tibial Block Augment...
The Issue: The implant only has one bolt in the sterile package but it should have had two.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Kerlix Gauze Roll Recalled by COVIDIEN LLC Due to Potential for product...
The Issue: Potential for product sterility breach due to a compromised or pinched seal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dermacea Gauze Fluff Roll Recalled by COVIDIEN LLC Due to Potential for...
The Issue: Potential for product sterility breach due to a compromised or pinched seal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dermacea Gauze Fluff Roll Recalled by COVIDIEN LLC Due to Potential for...
The Issue: Potential for product sterility breach due to a compromised or pinched seal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Kerlix Bandage Roll Recalled by COVIDIEN LLC Due to Potential for product...
The Issue: Potential for product sterility breach due to a compromised or pinched seal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Kerlix AMD Antimicrobial Bandage Roll Recalled by COVIDIEN LLC Due to...
The Issue: Potential for product sterility breach due to a compromised or pinched seal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: sterEOS workstation Recalled by EOS Imaging Due to 3D projections may be...
The Issue: 3D projections may be incorrect when the pair of images used is a secondary...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hemosll ReadiPlasTin (10 mL Size) Recalled by Instrumentation Laboratory Co....
The Issue: There is a potential for increased imprecision, out of range quality...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Kerlix Bandage Roll Recalled by COVIDIEN LLC Due to Potential for product...
The Issue: Potential for product sterility breach due to a compromised or pinched seal...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Plum 360 Infusion System With MedNet/ Smart Card Plug And Play Module...
The Issue: A software malfunction of the infuser when used with a MedNet Custom Drug...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alcon Air Optix Night & Day Aqua (lotrafilcon A) Recalled by Allied Vision...
The Issue: Potentially counterfeit products in/and counterfeit packaging were imported...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CAPNOSTREAM 20P (US) N - ROHS Recalled by Oridion Medical 1987 Ltd. Due to...
The Issue: The date/time, nurse call and alarm settings of the bedside patient monitors...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Capnostream20 (INTL) M W/PRINTER Recalled by Oridion Medical 1987 Ltd. Due...
The Issue: The date/time, nurse call and alarm settings of the bedside patient monitors...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CAPNOSTREAM 20P (INTL) N W/PRINTER - ROHS Recalled by Oridion Medical 1987...
The Issue: The date/time, nurse call and alarm settings of the bedside patient monitors...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Capnostream20 (US) N W/PRINTER Recalled by Oridion Medical 1987 Ltd. Due to...
The Issue: The date/time, nurse call and alarm settings of the bedside patient monitors...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Capnostream20 M W/PRINTER CYVITAL Recalled by Oridion Medical 1987 Ltd. Due...
The Issue: The date/time, nurse call and alarm settings of the bedside patient monitors...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Capnostream20 N CYVITAL Recalled by Oridion Medical 1987 Ltd. Due to The...
The Issue: The date/time, nurse call and alarm settings of the bedside patient monitors...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.