Product Recalls in Massachusetts

Product recalls affecting Massachusetts — including food, drugs, consumer products, medical devices, and vehicles distributed to Massachusetts. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,678 recalls have been distributed to Massachusetts in the last 12 months.

52,647 total recalls
2,678 in last 12 months

Showing 1338113400 of 13,418 recalls

DrugMarch 9, 2012· Pack Pharmaceuticals

Recalled Item: Ciprofloxacin Tablets Recalled by Pack Pharmaceuticals Due to Labeling...

The Issue: Labeling Illegible: Missing Label; The voluntary recall of the...

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

Class III — Low RiskOngoing
Refund
DrugFebruary 24, 2012· Lloyd Inc

Recalled Item: Levothroid (levothyroxine sodium tablets Recalled by Lloyd Inc Due to...

The Issue: Subpotent (Single Ingredient Drug): Low assay at the 6-month test interval.

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 24, 2012· Lloyd Inc

Recalled Item: Thyro-Tab.075 mg. Recalled by Lloyd Inc Due to Subpotent (Single Ingredient...

The Issue: Subpotent (Single Ingredient Drug): Low assay at the 6-month test interval.

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 23, 2012· www.vitaminbestbuy.com

Recalled Item: Man King Capsules Recalled by www.vitaminbestbuy.com Due to Marketed Without...

The Issue: Marketed Without an Approved ANDA/NDA: presence of sildenafil.

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

Class I — Serious Health HazardOngoing
Refund
DrugFebruary 23, 2012· www.vitaminbestbuy.com

Recalled Item: Hard Ten Days Capsule Recalled by www.vitaminbestbuy.com Due to Marketed...

The Issue: Marketed Without an Approved ANDA/NDA: presence of sildenafil

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

Class I — Serious Health HazardOngoing
Refund
DrugFebruary 23, 2012· www.vitaminbestbuy.com

Recalled Item: Japan Weight Loss Blue Capsules Recalled by www.vitaminbestbuy.com Due to...

The Issue: Marketed Without an Approved ANDA/NDA: presence of sibutramine

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

Class I — Serious Health HazardOngoing
Refund
DrugFebruary 6, 2012· sanofi-aventis US, Inc.

Recalled Item: Eloxatin (OXALIplatin injection) 5 mg/mL injection Recalled by...

The Issue: CGMP Deviations: Eloxatin was manufactured by Ben Venue Laboratories, a...

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 6, 2012· sanofi-aventis US, Inc.

Recalled Item: Eloxatin (OXALIplatin injection) 5 mg/mL Injection Recalled by...

The Issue: CGMP Deviations: Eloxatin was manufactured by Ben Venue Laboratories, a...

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 3, 2012· Lloyd Inc

Recalled Item: Levothroid (levothyroxine sodium tablets Recalled by Lloyd Inc Due to...

The Issue: Subpotent (Single Ingredient Drug): Low assay at the 9-month test interval.

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 3, 2012· Lloyd Inc

Recalled Item: Thyro-Tab 0.050mg. Recalled by Lloyd Inc Due to Subpotent (Single Ingredient...

The Issue: Subpotent (Single Ingredient Drug): Low assay at the 9-month test interval.

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 19, 2011· Body Basics Inc

Recalled Item: Actra-SX 500 Capsules Recalled by Body Basics Inc Due to Marketed without an...

The Issue: Marketed without an Approved NDA/ANDA; product contains sildenafil, an...

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

Class I — Serious Health HazardOngoing
Refund
DrugNovember 8, 2011· Carefusion 213, Llc

Recalled Item: ChloraPrep with Tint Recalled by Carefusion 213, Llc Due to Lack of...

The Issue: Lack of Assurance of Sterility: A customer complaint reported some units had...

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 17, 2011· Meda Pharmaceuticals Inc.

Recalled Item: Prefera OB One Gel Capsules Recalled by Meda Pharmaceuticals Inc. Due to...

The Issue: Labeling: Presence of Undeclared Color Additive; The product is being...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 30, 2011· VistaPharm, Inc.

Recalled Item: Xactdose Phenytoin Oral Suspension Recalled by VistaPharm, Inc. Due to...

The Issue: Defective container; lidding deformity allows the contained product to...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 27, 2011· Shamrock Medical Solutions Group LLC

Recalled Item: Oxycodone HCl Oral Concentrate Recalled by Shamrock Medical Solutions Group...

The Issue: Labeling: Label Mix up; product labeled as Morphine Sulfate 20 mg/mL...

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

Class I — Serious Health HazardOngoing
Refund
DrugSeptember 27, 2011· Shamrock Medical Solutions Group LLC

Recalled Item: Sulfamethoxazole and Trimethoprim Tablets Recalled by Shamrock Medical...

The Issue: Labeling: Label Mix up; product labeled to contain Sulfamethoxazole and...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 27, 2011· Shamrock Medical Solutions Group LLC

Recalled Item: metFORMIN ER Tablets Recalled by Shamrock Medical Solutions Group LLC Due to...

The Issue: Labeling: Label Mix up; product labeled did not indicated Extended Release

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

Class I — Serious Health HazardOngoing
Refund
DrugSeptember 27, 2011· Shamrock Medical Solutions Group LLC

Recalled Item: Pramipexole Dihydrochloride Tablets Recalled by Shamrock Medical Solutions...

The Issue: Labeling: Label Mix up; product labeled to contain Nebivolol tablets...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 27, 2011· Shamrock Medical Solutions Group LLC

Recalled Item: Docusate Calcium Softgel Capsules Recalled by Shamrock Medical Solutions...

The Issue: Labeling: Label Mix up; product labeled to contain Docusate Sodium 240mg...

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

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 27, 2011· Shamrock Medical Solutions Group LLC

Recalled Item: Taztia XT (Diltiazem HCl) Capsules Recalled by Shamrock Medical Solutions...

The Issue: Labeling: Label Mix Up; packages labeled as Thiamine actually contain...

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

Class I — Serious Health HazardOngoing
Refund