Product Recalls in Georgia

Product recalls affecting Georgia — including food, drugs, consumer products, medical devices, and vehicles distributed to Georgia. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,837 recalls have been distributed to Georgia in the last 12 months.

53,623 total recalls
2,837 in last 12 months

Showing 52215240 of 13,719 recalls

DrugNovember 1, 2019· KVK-Tech, Inc.

Recalled Item: Hydrocodone Bitartrate and Homatropine Methlybromide Oral Solution 5 mg/1.5...

The Issue: Presence of Foreign Substance: Black particles were found in the lots during...

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 31, 2019· Fagron, Inc

Recalled Item: LETS GEL KIT Convenience Pack (To prepare 100 mL LETS GEL) Recalled by...

The Issue: Microbial contamination of non-sterile product.

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 30, 2019· Avantor Performance Materials Inc

Recalled Item: Potassium Phosphate Recalled by Avantor Performance Materials Inc Due to...

The Issue: Failed Stability Specifications: Product exceeds compendia and firm's...

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 28, 2019· Lannett Company, Inc.

Recalled Item: Lannett Ranitidine Syrup (Ranitidine Oral Solution Recalled by Lannett...

The Issue: CGMP Deviations: Presence of NDMA impurity detected in product.

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 25, 2019· Novitium Pharma LLC

Recalled Item: Novitium Pharma Ranitidine Capsules 300 mg 100 capsules Rx Only Recalled by...

The Issue: CGMP Deviations: Presence of NDMA impurity detected in product.

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 25, 2019· ICU Medical Inc

Recalled Item: 0.9% SODIUM CHLORIDE INJECTION Recalled by ICU Medical Inc Due to Presence...

The Issue: Presence of Particulate Matter.

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

Class I — Serious Health HazardOngoing
Refund
DrugOctober 25, 2019· ICU Medical Inc

Recalled Item: LACTATED RINGER'S Injection Recalled by ICU Medical Inc Due to Presence of...

The Issue: Presence of Particulate Matter.

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

Class I — Serious Health HazardOngoing
Refund
DrugOctober 25, 2019· Novitium Pharma LLC

Recalled Item: Novitium Pharma Ranitidine Capsules 150 mg 500 capsules Rx Only Recalled by...

The Issue: CGMP Deviations: Presence of NDMA impurity detected in product.

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 25, 2019· Novitium Pharma LLC

Recalled Item: Novitium Pharma Ranitidine Capsules 150 mg 60 capsules Rx Only Recalled by...

The Issue: CGMP Deviations: Presence of NDMA impurity detected in product.

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 25, 2019· Novitium Pharma LLC

Recalled Item: Novitium Pharma Ranitidine Capsules 300 mg 30 capsules Rx Only Recalled by...

The Issue: CGMP Deviations: Presence of NDMA impurity detected in product.

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 23, 2019· Perrigo Company PLC

Recalled Item: Maximum Strength Acid Reducer Recalled by Perrigo Company PLC Due to CGMP...

The Issue: CGMP Deviation; Possible contamination with impurity N-nitrosodimethylamine.

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 23, 2019· Perrigo Company PLC

Recalled Item: Regular Strength Acid Reducer Recalled by Perrigo Company PLC Due to CGMP...

The Issue: CGMP Deviation; Possible contamination with impurity N-nitrosodimethylamine.

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 23, 2019· Perrigo Company PLC

Recalled Item: Maximum Strength Acid Reducer Recalled by Perrigo Company PLC Due to CGMP...

The Issue: CGMP Deviation; Possible contamination with impurity N-nitrosodimethylamine.

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 23, 2019· Perrigo Company PLC

Recalled Item: Regular Strength Acid Reducer Recalled by Perrigo Company PLC Due to CGMP...

The Issue: CGMP Deviation; Possible contamination with impurity N-nitrosodimethylamine.

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 23, 2019· Perrigo Company PLC

Recalled Item: Maximum Strength Acid Reducer Recalled by Perrigo Company PLC Due to CGMP...

The Issue: CGMP Deviation; Possible contamination with impurity N-nitrosodimethylamine.

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 23, 2019· Perrigo Company PLC

Recalled Item: Maximum Strength Acid Reducer Recalled by Perrigo Company PLC Due to CGMP...

The Issue: CGMP Deviation; Possible contamination with impurity N-nitrosodimethylamine.

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 23, 2019· Perrigo Company PLC

Recalled Item: Maximum Strength Acid Reducer Recalled by Perrigo Company PLC Due to CGMP...

The Issue: CGMP Deviation; Possible contamination with impurity N-nitrosodimethylamine.

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 23, 2019· Perrigo Company PLC

Recalled Item: Regular Strength Acid Reducer Recalled by Perrigo Company PLC Due to CGMP...

The Issue: CGMP Deviation; Possible contamination with impurity N-nitrosodimethylamine.

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 23, 2019· Perrigo Company PLC

Recalled Item: Maximum Strength Acid Reducer Recalled by Perrigo Company PLC Due to CGMP...

The Issue: CGMP Deviation; Possible contamination with impurity N-nitrosodimethylamine.

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 23, 2019· Perrigo Company PLC

Recalled Item: Maximum Strength Acid Reducer Recalled by Perrigo Company PLC Due to CGMP...

The Issue: CGMP Deviation; Possible contamination with impurity N-nitrosodimethylamine.

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

Class II — Potential Health HazardOngoing
Refund