Product Recalls in Colorado

Product recalls affecting Colorado — including food, drugs, consumer products, medical devices, and vehicles distributed to Colorado. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,652 recalls have been distributed to Colorado in the last 12 months.

51,434 total recalls
2,652 in last 12 months

Showing 1346113480 of 13,494 recalls

DrugFebruary 20, 2012· Physicians Total Care, Inc.

Recalled Item: PHYSICIANS TOTAL CARE Recalled by Physicians Total Care, Inc. Due to...

The Issue: Presence of Foreign Substance(s): There is a potential for foreign...

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

Class II — Potential Health HazardOngoing
Refund
DrugFebruary 20, 2012· Physicians Total Care, Inc.

Recalled Item: PHYSICIANS TOTAL CARE Recalled by Physicians Total Care, Inc. Due to...

The Issue: Presence of Foreign Substance(s): There is a potential for foreign...

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 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: 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: 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
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: 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: 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
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