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. 2,558 recalls have been distributed to Mississippi in the last 12 months.
Showing 16141–16160 of 28,172 recalls
Recalled Item: Draco Enzymatic Deep-Cleaning Pad Recalled by Madison Polymeric Engineering...
The Issue: The products exhibit an unpleasant odor due to microbial contamination with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: First Step Endoscopic Cleaning Pad Recalled by Madison Polymeric Engineering...
The Issue: The products exhibit an unpleasant odor due to microbial contamination with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Travel Kit Recalled by Madison Polymeric Engineering Due to The products...
The Issue: The products exhibit an unpleasant odor due to microbial contamination with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: First Step Endoscopic Cleaning Pad Recalled by Madison Polymeric Engineering...
The Issue: The products exhibit an unpleasant odor due to microbial contamination with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: First Step Endoscopic Cleaning Pad Recalled by Madison Polymeric Engineering...
The Issue: The products exhibit an unpleasant odor due to microbial contamination with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: First Step Endoscopic Cleaning Pad with 4" Button Brush Recalled by Madison...
The Issue: The products exhibit an unpleasant odor due to microbial contamination with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dimension Vista¿ MULTI 1 SDIL Recalled by Siemens Healthcare Diagnostics,...
The Issue: The diluent may have an incomplete slit on the septum in the cap of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dimension Vista¿ CTNI Sample Diluent Recalled by Siemens Healthcare...
The Issue: The diluent may have an incomplete slit on the septum in the cap of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bard Midstream Urine Collector with Rigid Funnel and Iodophor Prep Recalled...
The Issue: Medline notified BMD that the Aplicare Povidone Iodine (PVP-I) Prep Pads...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Vacutainer¿ Push Button Blood Collection Set 0.6 x 19 Recalled by Becton...
The Issue: Products do not meet the labeled sterility claim of a Sterility Assurance...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: First aid/emergency kits containing Honeywell eyewash: CSM kit number...
The Issue: Firm is recalling first aid/emergency kits and cabinets which contain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Vacutainer¿ Ultra TouchTM Push Button Blood Collection Set 0.6 Recalled...
The Issue: Products do not meet the labeled sterility claim of a Sterility Assurance...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Vacutainer¿ Push Button Blood Collection Set 0.8 x 19 Recalled by Becton...
The Issue: Products do not meet the labeled sterility claim of a Sterility Assurance...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stem Extractor f/Guide Bar Recalled by Synthes, Inc. Due to There is a...
The Issue: There is a potential for the connection screw of the stem extractor to break.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Intera 0.5T Standard Recalled by Philips Electronics North America...
The Issue: Potential risk for helium gas inside the MR examination room during a magnet...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Multiva systems Recalled by Philips Electronics North America Corporation...
The Issue: Potential risk for helium gas inside the MR examination room during a magnet...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Conversion SmarthPath to dStream for 1.5T Recalled by Philips Electronics...
The Issue: Potential risk for helium gas inside the MR examination room during a magnet...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Achieva 1.5T: 1) Nova (Dual) Recalled by Philips Electronics North America...
The Issue: Potential risk for helium gas inside the MR examination room during a magnet...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: T5-NT Recalled by Philips Electronics North America Corporation Due to...
The Issue: Potential risk for helium gas inside the MR examination room during a magnet...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nobel Biocare 17¿ Multi-Unit Abutment Recalled by Nobel Biocare Usa Llc Due...
The Issue: The product label has missing information, such as the lot number and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.