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. 2,411 recalls have been distributed to Mississippi in the last 12 months.

49,744 total recalls
2,411 in last 12 months

Showing 4136141380 of 49,744 recalls

Medical DeviceJune 30, 2014· Steris Corporation

Recalled Item: Reliance 1227 Cart and Utensil Washer/Disinfector Product Usage: Usage: The...

The Issue: STERIS has identified that deformation of the washers door handle pin may...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class III — Low RiskOngoing
DrugJune 27, 2014· Hospira Inc.

Recalled Item: Fentanyl Citrate Injection Recalled by Hospira Inc. Due to Lack of Assurance...

The Issue: Lack of Assurance of Sterility: Fliptop vial crimps are loose or missing.

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJune 27, 2014· Life Force of Tampa, LLC

Recalled Item: Life Force Chamber Product Usage:The product is intended for restful...

The Issue: The Life Force chamber is marketed and promoted as a medical device,...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 27, 2014· Brainlab AG

Recalled Item: Patient Data Manager 2.0 (Content manager 2.0 Recalled by Brainlab AG Due to...

The Issue: The following defects have been identified for data loaded with Patient Data...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 27, 2014· Steris Corporation

Recalled Item: The STERIS 4085 General Surgical Table Product Usage: is an Recalled by...

The Issue: STERIS engineering analysis has determined the D1 pressure switch in the...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
DrugJune 26, 2014· Caraco Pharmaceutical Laboratories, Ltd.

Recalled Item: Cephalexin Capsules Recalled by Caraco Pharmaceutical Laboratories, Ltd. Due...

The Issue: CGMP Deviations: These products are being recalled because they were...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugJune 26, 2014· Caraco Pharmaceutical Laboratories, Ltd.

Recalled Item: Cephalexin Capsules Recalled by Caraco Pharmaceutical Laboratories, Ltd. Due...

The Issue: CGMP Deviations: These products are being recalled because they were...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugJune 26, 2014· Poly Pharmaceuticals, Inc

Recalled Item: LORTUSS EX Recalled by Poly Pharmaceuticals, Inc Due to Does Not Meet...

The Issue: Does Not Meet Monograph: Phenylephrine and pseudoephedrine are below...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
DrugJune 26, 2014· Poly Pharmaceuticals, Inc

Recalled Item: POLY-TUSSIN AC LIQUID Recalled by Poly Pharmaceuticals, Inc Due to Does Not...

The Issue: Does Not Meet Monograph: Phenylephrine and pseudoephedrine are below...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class III — Low RiskOngoing
Refund
Medical DeviceJune 26, 2014· Hill-Rom, Inc.

Recalled Item: Affinity¿ Four Birthing Bed Recalled by Hill-Rom, Inc. Due to The attachment...

The Issue: The attachment latch mechanism can become bent depending on user handling....

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 26, 2014· Alphatec Spine, Inc.

Recalled Item: Solanas 2.1mm FIXED DEPTH DRILL Recalled by Alphatec Spine, Inc. Due to...

The Issue: Alphatec Spine is recalling the 2.1mm Fixed Depth Drill 10mm because they...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJune 26, 2014· Biosound Esaote, Inc.

Recalled Item: Esaote PA230E Transducer A portable and cart base ultrasound system Recalled...

The Issue: Using the PA230E transducer with a user-defined setting with the output...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
DrugJune 25, 2014· Medical Supply Liquidators Llc

Recalled Item: G.A.C. 375 Injection USP Recalled by Medical Supply Liquidators Llc Due to...

The Issue: Marketed without an Approved NDA/ANDA; IM and SQ injectable products are...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugJune 25, 2014· Medical Supply Liquidators Llc

Recalled Item: Vitamin B12 Hydroxocobalamin Injection USP 1000 mcg/ml Recalled by Medical...

The Issue: Marketed without an Approved NDA/ANDA; IM and SQ injectable products are...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugJune 25, 2014· Medical Supply Liquidators Llc

Recalled Item: BCAA 4% Branched Chain Amino Acid Injection USP Recalled by Medical Supply...

The Issue: Marketed without an Approved NDA/ANDA; IM and SQ injectable products are...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugJune 25, 2014· Medical Supply Liquidators Llc

Recalled Item: Glutathione Injection USP Recalled by Medical Supply Liquidators Llc Due to...

The Issue: Marketed without an Approved NDA/ANDA; IM and SQ injectable products are...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugJune 25, 2014· Medical Supply Liquidators Llc

Recalled Item: Vitamin B12 Methylcobalamin 5000 Injection USP 5000 mcg/ml Recalled by...

The Issue: Marketed without an Approved NDA/ANDA; IM and SQ injectable products are...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugJune 25, 2014· Medical Supply Liquidators Llc

Recalled Item: L-Carnitine Injection USP 100 mg/ml Recalled by Medical Supply Liquidators...

The Issue: Marketed without an Approved NDA/ANDA; IM and SQ injectable products are...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugJune 25, 2014· Medical Supply Liquidators Llc

Recalled Item: Super MIC B Complex for L-Carnitine for Injection USP with Recalled by...

The Issue: Marketed without an Approved NDA/ANDA; IM and SQ injectable products are...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugJune 25, 2014· Medical Supply Liquidators Llc

Recalled Item: Vitamin B12 Methylcobalamin Injection USP 1000 mcg/ml Recalled by Medical...

The Issue: Marketed without an Approved NDA/ANDA; IM and SQ injectable products are...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund