Product Recalls in New York

Product recalls affecting New York — including food, drugs, consumer products, medical devices, and vehicles distributed to New York. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,812 recalls have been distributed to New York in the last 12 months.

55,896 total recalls
2,812 in last 12 months

Showing 1356113580 of 13,591 recalls

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: 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 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 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: 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
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
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
DrugJuly 6, 2011· Bausch & Lomb, Inc.

Recalled Item: Murocel (methylcellulose) Lubricant Opthalmic Solution (USP Recalled by...

The Issue: Lack of Assurance of Sterility: Bausch & Lomb, Inc. is recalling 7 Lots of...

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 5, 2011· Noven Pharmaceuticals, Inc.

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

The Issue: Miscalibrated and/or Defective Delivery System: Out of Specification results...

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 5, 2011· Noven Pharmaceuticals, Inc.

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

The Issue: Miscalibrated and/or Defective Delivery System: Out of Specification results...

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 5, 2011· Noven Pharmaceuticals, Inc.

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

The Issue: Miscalibrated and/or Defective Delivery System: Out of Specification results...

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

Class II — Potential Health HazardOngoing
Refund
DrugJuly 5, 2011· Noven Pharmaceuticals, Inc.

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

The Issue: Miscalibrated and/or Defective Delivery System: Out of Specification results...

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 22, 2011· Nephron Pharmaceuticals Corp.

Recalled Item: Albuterol Sulfate Inhalation Solution Recalled by Nephron Pharmaceuticals...

The Issue: Lack of Assurance of Sterility

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

Class II — Potential Health HazardOngoing
Refund
DrugJune 15, 2011· Apotex Corp.

Recalled Item: Azelastine HCl Nasal Solution Recalled by Apotex Corp. Due to CGMP...

The Issue: CGMP Deviations: tubing used for filling may interact with the nasal...

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

Class III — Low RiskOngoing
Refund