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. 2,448 recalls have been distributed to Mississippi in the last 12 months.
Showing 26201–26220 of 28,172 recalls
Recalled Item: STERRAD 200 Sterilization System Recalled by Advanced Sterilization Products...
The Issue: The recall was initiated because Advanced Sterilization Products (ASP) has...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ORTHOCORD One Violet and One Blue Braided Composite Suture with Recalled by...
The Issue: The IFU provided with the free strand ORTHOCORD sutures currently indicates...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EVOTECH Endoscope Cleaner & Reprocessor System Recalled by Advanced...
The Issue: Advanced Sterilization Products (ASP) has determined that a limited number...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ORTHOCORD One Violet and One Blue Braided Composite Suture with Recalled by...
The Issue: The IFU provided with the free strand ORTHOCORD sutures currently indicates...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ORTHOCORD BLUE BRAIDED COMPOSITE SUTURE 2 (5 METRIC) Recalled by DePuy...
The Issue: The IFU provided with the free strand ORTHOCORD sutures currently indicates...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STERRAD 100NX Sterilization System Recalled by Advanced Sterilization...
The Issue: The recall was initiated because Advanced Sterilization Products (ASP) has...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LHB Recalled by Lighthouse For The Blind Due to The product contains an...
The Issue: The product contains an iodine 10% Ampule (10% Povidone Iodine swab) which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LHB Recalled by Lighthouse For The Blind Due to The product contains an...
The Issue: The product contains an iodine 10% Ampule (10% Povidone Iodine swab) which...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brilliance CT 64 Recalled by Philips Medical Systems (Cleveland) Inc Due to...
The Issue: If the operator selects a patient name from the worklist using the mouse and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The GemStar Pump is a small and lightweight Recalled by Hospira Inc. Due to...
The Issue: During infusions of 2.0 mL/hr the motor assembly may rotate backwards...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The GemStar Pump is a small and lightweight Recalled by Hospira Inc. Due to...
The Issue: During infusions of 2.0 mL/hr the motor assembly may rotate backwards...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HORIBA ABX PENTRA 400 I.S.E. Module Recalled by Horiba Instruments, Inc dba...
The Issue: HORIBA Medical is informing all ABX PENTRA 400 Analyzer with I.S.E. Module...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Oxford Uni Knee System Recalled by Biomet U.K., Ltd. Due to Investigation of...
The Issue: Investigation of complaints found excessive use of the instrument could...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Accuray CyberKnife System Medical Physicist Recalled by Accuray Incorporated...
The Issue: A defect on the master-side connector block of the pneumatic tool changer...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GemStar infusion pump Recalled by Hospira Inc. Due to Some patients are...
The Issue: Some patients are obtaining access to the dosage reset codes required to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GemStar infusion pump Recalled by Hospira Inc. Due to Some patients are...
The Issue: Some patients are obtaining access to the dosage reset codes required to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LeMaitre Stent Guide: 1102-00 (100 strips) Recalled by LeMaitre Vascular,...
The Issue: Devices were not sealed correctly during the manufacturing process, and the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Integra Ojemann Cortical Stimulator Recalled by Integra Burlington MA, Inc....
The Issue: If the headphone jack is in use during a surgical procedure with the OCS2...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Glow 'N Tell 20 cm Tape: 1100-00 (100 strips) Recalled by LeMaitre Vascular,...
The Issue: Devices were not sealed correctly during the manufacturing process, and the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PSS Select medical products***Biopsy Punches*** Disposable manual instrument...
The Issue: Due to lack of sterilization.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.