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. 1,075 recalls have been distributed to Mississippi in the last 12 months.
Showing 15861–15880 of 49,744 recalls
Recalled Item: ZVplasty Direct Access Diamond Tip Trocar Recalled by Zavation Due to...
The Issue: Products distributed as sterile may not have been adequately sterilized
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ZVplasty Direct Bipedicular Bone Access Kit with Drill Recalled by Zavation...
The Issue: Products distributed as sterile may not have been adequately sterilized
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 11G DIAMOND TROCAR/CANNULA. For use in Orthopedic / spinal procedures....
The Issue: Products distributed as sterile may not have been adequately sterilized
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ZVplasty System Recalled by Zavation Due to Products distributed as sterile...
The Issue: Products distributed as sterile may not have been adequately sterilized
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VERTEBREX SINGLE BALLOON KIT Recalled by Zavation Due to Products...
The Issue: Products distributed as sterile may not have been adequately sterilized
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 10 GAUGE SINGLE CEMENT DELIVERY 4 FILLERS 4 SYRINGES Recalled by Zavation...
The Issue: Products distributed as sterile may not have been adequately sterilized
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 10G CEMENT DELIVERY CANNULA. For use in Orthopedic / spinal procedures....
The Issue: Products distributed as sterile may not have been adequately sterilized
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 10 Gauge Drill Recalled by Zavation Due to Products distributed as sterile...
The Issue: Products distributed as sterile may not have been adequately sterilized
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 11G DIRECT SINGLE - DELIVERY (4 FILLERS-4 SYRINGES) CODE: INTVMN-SCDK....
The Issue: Products distributed as sterile may not have been adequately sterilized
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: InterV CurvePlus Kit Recalled by Zavation Due to Products distributed as...
The Issue: Products distributed as sterile may not have been adequately sterilized
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ZVplasty System Recalled by Zavation Due to Products distributed as sterile...
The Issue: Products distributed as sterile may not have been adequately sterilized
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 10G DIRECT DOUBLE BONE ACCESS KIT. For use in Orthopedic / spinal...
The Issue: Products distributed as sterile may not have been adequately sterilized
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 10 GAUGE SINGLE CEMENT DELIVERY 4 FILLERS 4 SYRINGES STERILE. Recalled by...
The Issue: Products distributed as sterile may not have been adequately sterilized
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: cobas Liat Analyzer: respiratory virus panel nucleic acid assay system...
The Issue: Invalid or false positive results for one or more targets...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Aftermarket Alaris Infusion Pump Module Model 8100 Front Bezel Recalled by...
The Issue: Aftermarket front bezel components were installed during service/repair, not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BioGX SARS-CoV-2 Reagents for BD MAX System-IVD PCR test intended Recalled...
The Issue: BioGX SARS-CoV-2 Reagents for BD MAX" System rehydration buffer tubes were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Drop Arm Versamode" Recalled by Gf Health Products Due to The front casters...
The Issue: The front casters on the 6810A Lumex Drop Arm Versamode are incorrect.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Thumbs Up 7 Blue 69K Recalled by Bit & Bet LLC Due to Marketed without...
The Issue: Marketed without Approved NDA/ANDA: FDA analysis results obtained the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: VenaSeal Closure System Recalled by Medtronic Inc. Due to Firm received...
The Issue: Firm received increased number of reports that VenaSeal dispensing systems...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BPB medica CEMIX Recalled by BIOPSYBELL S.R.L. Due to Products labeled as...
The Issue: Products labeled as sterile were distributed, but may not have been sterilized.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.