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 48614880 of 13,719 recalls

DrugMarch 16, 2020· PharMEDium Services, LLC

Recalled Item: nICARdipine HCl (0.1 mg/mL) 1 mg/10mL Recalled by PharMEDium Services, LLC...

The Issue: Firm is recalling 46 lots of various products because of a lack of sterility...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 13, 2020· Sun Pharmaceutical Industries, Inc.

Recalled Item: Doxycycline Capsules Recalled by Sun Pharmaceutical Industries, Inc. Due to...

The Issue: CGMP Deviations: Doxycycline capsules were not manufactured under Current...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 13, 2020· Sun Pharmaceutical Industries, Inc.

Recalled Item: Doxycycline Capsules Recalled by Sun Pharmaceutical Industries, Inc. Due to...

The Issue: CGMP Deviations: Doxycycline capsules were not manufactured under Current...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 11, 2020· Jubilant Cadista Pharmaceuticals, Inc.

Recalled Item: Pantoprazole Sodium Delayed-Release Tablets Recalled by Jubilant Cadista...

The Issue: CGMP Deviations: Presence of dark brown discoloration on edges of tablets

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 9, 2020· Mylan Pharmaceuticals Inc.

Recalled Item: Sotalol HCL Tablets Recalled by Mylan Pharmaceuticals Inc. Due to Presence...

The Issue: Presence of particulate matter. presence of metal particles.

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 9, 2020· Sun Pharmaceutical Industries, Inc.

Recalled Item: Atorvastatin Calcium Tablets Recalled by Sun Pharmaceutical Industries, Inc....

The Issue: Presence of foreign substance: Foreign matter has been identified as latex...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 9, 2020· Lupin Pharmaceuticals Inc.

Recalled Item: Levonorgestrel and Ethinyl Estradiol Tablets USP Recalled by Lupin...

The Issue: Failed Content Uniformity Specifications: Out Of Specification test results...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 9, 2020· Lupin Pharmaceuticals Inc.

Recalled Item: Bekyree (desogestrel and ethinyl estradiol tablets USP Recalled by Lupin...

The Issue: Failed Content Uniformity Specifications: Out Of Specification test results...

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

Class III — Low RiskOngoing
Refund
DrugMarch 6, 2020· H J Harkins Company Inc dba Pharma Pac

Recalled Item: Acetaminophen 500 mg tablet packaged in a) 30-count bottles ( NDC...

The Issue: Presence of Foreign Tablets/Capsules: Complaint involving one Women's...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 4, 2020· Par Pharmaceutical Inc.

Recalled Item: PrediniSONE Tablets Recalled by Par Pharmaceutical Inc. Due to Labeling:...

The Issue: Labeling: Incorrect or Missing Exp Date - An incorrect expiration date has...

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

Class III — Low RiskOngoing
Refund
DrugMarch 3, 2020· Yusef Manufacturing Laboratories, LLC

Recalled Item: PEPPERMINT LIP MOISTURIZER (oxybenzone (4%) and Octinoxate (7%) SPF 15...

The Issue: Superpotent drug: This lot of SPF containing lip balm contains up to 150% of...

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 2, 2020· Noven Therapeutics, LLC

Recalled Item: Daytrana (methylphenidate transdermal system) patches Recalled by Noven...

The Issue: Defective Delivery System: Out of specification for mechanical peel and shear.

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 2, 2020· Noven Therapeutics, LLC

Recalled Item: Daytrana (methylphenidate transdermal system) patches Recalled by Noven...

The Issue: Defective Delivery System: Out of specification for mechanical peel and shear.

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 2, 2020· Noven Therapeutics, LLC

Recalled Item: Daytrana (methylphenidate transdermal system) patches Recalled by Noven...

The Issue: Defective Delivery System: Out of specification for mechanical peel and shear.

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 2, 2020· Noven Therapeutics, LLC

Recalled Item: Daytrana (methylphenidate transdermal system) patches Recalled by Noven...

The Issue: Defective Delivery System: Out of specification for mechanical peel and shear.

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

Class II — Potential Health HazardOngoing
Refund
DrugMarch 2, 2020· Mayne Pharma Inc

Recalled Item: Carbidopa and Levodopa Tablets Recalled by Mayne Pharma Inc Due to Product...

The Issue: Product Mix-Up: A foreign tablet was found in bottle.

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 27, 2020· The Harvard Drug Group

Recalled Item: Quetiapine Fumarate Extended-Release Tablets Recalled by The Harvard Drug...

The Issue: Labeling; Incorrect or Missing Package Insert: Product was packaged with the...

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

Class III — Low RiskOngoing
Refund
DrugFebruary 27, 2020· The Harvard Drug Group

Recalled Item: Quetiapine Fumarate Extended-Release Tablets Recalled by The Harvard Drug...

The Issue: Labeling; Incorrect or Missing Package Insert: Product was packaged with the...

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

Class III — Low RiskOngoing
Refund
DrugFebruary 27, 2020· The Harvard Drug Group

Recalled Item: Quetiapine Fumarate Extended-Release Tablets Recalled by The Harvard Drug...

The Issue: Labeling; Incorrect or Missing Package Insert: Product was packaged with the...

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

Class III — Low RiskOngoing
Refund
DrugFebruary 27, 2020· The Harvard Drug Group

Recalled Item: Quetiapine Fumarate Extended-Release Tablets Recalled by The Harvard Drug...

The Issue: Labeling; Incorrect or Missing Package Insert: Product was packaged with the...

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

Class III — Low RiskOngoing
Refund