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. 2,394 recalls have been distributed to Mississippi in the last 12 months.
Showing 43221–43240 of 49,744 recalls
Recalled Item: MINERAL IV Injection Recalled by Abrams Royal Pharamacy Due to...
The Issue: Non-Sterility; analytical results found product to contain Sphingomonas...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: All Unexpired Sterile Drug Products Recalled by Abrams Royal Pharamacy Due...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Brilliance CT Big Bore Oncology Whole Body Computed Tomography X-Ray...
The Issue: During internal testing, the Brilliance CT Big Bore was found to be out of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VERIFY¿ SixCess 270FP Challenge Pack Recalled by Steris Corporation Due to...
The Issue: STERIS has identified that the outer shipping package for one lot (Lot...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Single and Dual use Emission Computer Tomography gamma cameras (BrightView...
The Issue: Three problems were reported to the firm: When positioning for a relative...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hemochron Jr. Citrate APTT Cuvette 510(k) K014008 A unitized...
The Issue: ITC has determined that some Citrate APTT cuvettes may recover higher than...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARIATELE TELEMETRY TRANSMITTER Recalled by Spacelabs Healthcare, Llc Due to...
The Issue: The AriaTele Model 96281 with SpO2 monitoring Option C is recalled because...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zimmer Segmental Systems Recalled by Zimmer, Inc. Due to After evaluation of...
The Issue: After evaluation of 13 complaints(0.4% rate) for hyper-extension of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Zimmer Segmental Systems Recalled by Zimmer, Inc. Due to After evaluation of...
The Issue: After evaluation of 13 complaints(0.4% rate) for hyper-extension of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Weck Recalled by Teleflex Medical Due to Sterility cannot be guaranteed.
The Issue: Sterility cannot be guaranteed.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Weck Recalled by Teleflex Medical Due to Sterility cannot be guaranteed.
The Issue: Sterility cannot be guaranteed.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hydralazine HCL Tablets Recalled by Teva Pharmaceuticals USA Due to Failed...
The Issue: Failed Impurities/Degradation Specifications:There is a potential for the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Hydralazine HCL Tablets Recalled by Teva Pharmaceuticals USA Due to Failed...
The Issue: Failed Impurities/Degradation Specifications:There is a potential for the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Benefiber fiber supplement stick packs Recalled by Novartis Consumer Health...
The Issue: The products are being recalled due to the receipt of a relatively high...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: ROSA Surgical Device 2.5.8 ROSA Surgical Device is a computer-controlled...
The Issue: Possible break in the connector of the Force Sensor.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Specialty Straight Static Inserter Assembly Product Usage: This instrument...
The Issue: Stryker has received complaints from customers relating to fracture along...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA Centaur¿ Systems Phenytoin Calibrator N ( PHTN) 2-pack SMN Recalled by...
The Issue: ADVIA Centaur¿ Systems Phenytoin Calibrator N, lots CN58 and higher, change...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA Centaur¿ Systems Phenytoin Calibrator N ( PHTN) 6-pack SMN Recalled by...
The Issue: ADVIA Centaur¿ Systems Phenytoin Calibrator N, lots CN58 and higher, change...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ABX PENTRA Urine Control L/H. The ABX PENTRA Urine Control Recalled by...
The Issue: HORIBA Medical is informing all ABX PENTRA Urine Control L/H customers...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Boston Scientific Extractor Pro XL Retrieval Balloon Catheter 12-15 mm...
The Issue: Extractor Pro XL Retrieval Balloon Catheters may have the incorrect skive...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.