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 28221–28240 of 49,744 recalls
Recalled Item: Hypodermic Needle Recalled by International Medsurg Connection, Inc. Due to...
The Issue: Insufficient documentation to support product sterility claims.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OptiLITE(TM) Products for Laser Surgery Recalled by Xintec Corp Due to It...
The Issue: It has been determined that the reprocessing instructions may not provide...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Latanoprost PF Solution Recalled by ImprimisRx CA, Inc., dba ImprimisRx Due...
The Issue: Incorrect/Undeclared Excipient; non-pharmaceutical grade PEG 40 Castor Oil...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Timolol-Brimonidine-Dorzolamide-Latanoprost (0.5/0.15/2/0.005)% Ophthalmic...
The Issue: Incorrect/Undeclared Excipient; non-pharmaceutical grade PEG 40 Castor Oil...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Curcumin Emulsion 10mg/ml Injection Recalled by ImprimisRx CA, Inc., dba...
The Issue: Incorrect/Undeclared Excipient; non-pharmaceutical grade PEG 40 Castor Oil...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Timolol-Latanoprost PF Solution (0.5-0.005)% Recalled by ImprimisRx CA,...
The Issue: Incorrect/Undeclared Excipient; non-pharmaceutical grade PEG 40 Castor Oil...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Potassium Phosphate (USP) QS 0.9% Sodium Chloride (USP) 250 mL Recalled by...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Potassium Phosphate (USP) QS 0.9% Sodium Chloride (USP) 250 mL Recalled by...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Potassium Phosphate (USP) QS 0.9% Sodium Chloride (USP) 250 mL Recalled by...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: MAN OF STEEL capsules Recalled by Vitility Due to Undeclared Sildenafil
The Issue: Marketed Without An Approved NDA/ANDA: FDA analysis found this product to...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Paroxetine Extended-Release Tablets USP Recalled by Lupin Pharmaceuticals...
The Issue: Failed Dissolution Specifications: out of specification observed in...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: QUELICIN (Succinylcholine Chloride) Injection Recalled by Advanced Pharma...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: DLP Antegrade/Retrograde Adapter Method for perfusion of cardioplegia...
The Issue: Identification of small pinholes in a single packaging configuration of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DLP Cardioplegia Adapter with Pressure Port Provides access for a Recalled...
The Issue: Identification of small pinholes in a single packaging configuration of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DLP Pressure Disposable Pressure Display Sets Extends the pressure line...
The Issue: Identification of small pinholes in a single packaging configuration of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: InflammaDry(R) AN RPS DIAGNOSTIC SOLUTION Recalled by Quidel Corporation Due...
The Issue: In-house testing revealed the presence of plastic spurs at the tips of some...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DLP Pressure Monitoring Extension Line Adapters Extends the pressure line...
The Issue: Identification of small pinholes in a single packaging configuration of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The GC80 Digital X-ray Imaging System Recalled by NeuroLogica Corporation...
The Issue: An image was obtained with over exposure during a Thorax examination using...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DLP Extension Line Adapters 20 in length Used to extend Recalled by...
The Issue: Identification of small pinholes in a single packaging configuration of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PALLAS M/MAXIMIS 45mm MIS . Part of MAXIMIS Pedicle Screw Recalled by...
The Issue: Devices are not consistent with Quality System Requirements.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.