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Bracco Diagnostic Inc

Bracco Diagnostic Inc Recalls

All product recalls associated with Bracco Diagnostic Inc.

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Recall Summary

Total Recalls

1000

Past Year

304

Class I (Serious)

Most Recent

Nov 2025

Data from FDA, USDA, CPSC, and NHTSA public records. Recall counts vary by company size, industry, and reporting practices. Always check official sources for current information.

Showing 4181–4200 of 4747 recalls

Choletec Kit (Bracco) – Particulate Matter Risk (2012)

Presence of Particulate Matter; potential for charcoal particulates

Class IIILow

FDAAug 14, 2012Nationwide• Bracco Diagnostic Inc

Prometh VC with Codeine (Actavis) – Stability Degradation (2012)

Impurities/Degradation Products: Recalled lots do not meet room temperature stability specification for unknown degradant.

Class IIILow

FDAAug 14, 2012Nationwide• Actavis Mid Atlantic LLC

Prometh VC Plain (Actavis) – Stability Degradation (2012)

Impurities/Degradation Products: Recalled lots do not meet room temperature stability specification for unknown degradant.

Class III

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Low

FDAAug 14, 2012Nationwide• Actavis Mid Atlantic LLC

Fresh Mahi Mahi Fillets (Atlantic Fisheries) – High Histamine (2012)

Atlantic Fisheries recalled 580 lbs of Mahi Mahi Fillets due to histamine levels over 50 ppm.

Class IIModerate

FDAAug 13, 2012AL, FL, IN +1 more• Atlantic Fisheries

Doxazosin Tablets (Mylan) – Product Cross Contamination (2012)

Cross Contamination w/Other Products: During stability testing chromatographic review revealed extraneous peaks identified as acetaminophen and codeine.

Class IIModerate

FDAAug 7, 2012Nationwide• Mylan Pharmaceuticals Inc.

Levetiracetam Tablets (Mylan) – Foreign Tablet Presence (2012)

Adulterated Presence of Foreign Tablets: Pharmaceutical manufacturer may have distributed foreign tablets in bottles of Levetiracetam Tablets, USP 500 mg.

Class IIModerate

FDAJul 27, 2012KY• Mylan Pharmaceuticals Inc.

OFIRMEV Acetaminophen Injection (Cadence) – Particulate Matter (2012)

Presence of Particulate Matter: The firm initiated the recall due to visible presence of particulate matter.

Class IIModerate

FDAJul 24, 2012Nationwide• Cadence Pharmaceuticals

Ketoconazole Cream 2% (Fougera) – Specification Failure (2012)

Failed Impurities/Degradation Specifications: Ketoconazole Cream 2% is the subject of a voluntary drug recall by Fougera due to an Out Of Specification result for an unknown degradant product

Class IIILow

FDAJul 18, 2012Nationwide• Fougera Pharmaceuticals Inc.

Raspberry Filled Cake (Authentic Gourmet) – non-permitted ingredient (2012)

The recall was initiated because Authentic Gourmet was alerted by FDA sample analysis that the Strawberry Cake and the Raspberry Cake has non-permitted color additive and allergen, cochineal red A (also known as ponceau 4R).

Class IIModerate

FDAJul 13, 2012CA• Authentic Gourmet

Strawberry Filled Cake (Authentic Gourmet) – non-permitted ingredient (2012)

Class IIModerate

FDAJul 13, 2012CA• Authentic Gourmet

CosMedix Serious Protection Sunscreen (Covalence) – mold contamination (2012)

Microbial Contamination of Non Sterile Product; mold

Class IIModerate

FDAJul 13, 2012GA• Island Kinetics dba Covalence

Daytrana Patch 15mg (Noven) – delivery system defect (2012)

Miscalibrated and/or Defective Delivery System: Out of Specification results for mechanical peel force and/or the z-statistic value which relates to the patient's ability to remove the release liner from the patch adhesive prior to administration.

Class IIModerate

FDAJul 12, 2012Nationwide• Noven Pharmaceuticals, Inc.

Daytrana Patch 20mg (Noven) – delivery system defect (2012)

Class IIModerate

FDAJul 12, 2012Nationwide• Noven Pharmaceuticals, Inc.

Infants' Mapap Acetaminophen (Axcentria) – incorrect expiration (2012)

Labeling; labeled with incorrect EXP Date; Incorrect expiration date printed on the outer packaging. Package incorrectly states 5/2014 should correctly state 4/2014

Class IIILow

FDAJul 12, 2012MI• Axcentria Pharmaceuticals LLC

Daytrana Patch 30mg (Noven) – delivery system defect (2012)

Class IIModerate

FDAJul 12, 2012Nationwide• Noven Pharmaceuticals, Inc.

Chocolate Dipped Bars (Arctic Zero) – Undeclared Milk (2012)

Undeclared Milk

Arctic Zero Inc. is recalling their Arctic Zero Frozen Dessert products due to undeclared milk.

Class IHigh

FDAJul 6, 2012Nationwide• Arctic Zero, Inc.

Chocolate Peanut Butter (Arctic Zero) – Undeclared Milk (2012)

Undeclared Milk

Arctic Zero Inc. is recalling their Arctic Zero Frozen Dessert products due to undeclared milk.

Class IHigh

FDAJul 6, 2012Nationwide• Arctic Zero, Inc.

Hydrocortisone Acetic Acid Otic Solution (Vintage Pharmaceuticals) – impurity risk (2012)

Impurities/Degradation Products: Out of specificiation results for impurities at the 18-month room temperature time point.

Class IIILow

FDAJul 6, 2012Nationwide• Vintage Pharmaceuticals LLC DBA Qualitest Pharmaceuticals

Strawberry Orange Cream Bars (Arctic Zero) – Undeclared Milk (2012)

Undeclared Milk

Arctic Zero Inc. is recalling their Arctic Zero Frozen Dessert products due to undeclared milk.

Class IHigh

FDAJul 6, 2012Nationwide• Arctic Zero, Inc.

Mint Chocolate Cookie Frozen Dessert (Arctic Zero) – undeclared milk (2012)

Undeclared Milk

Arctic Zero Inc. is recalling their Arctic Zero Frozen Dessert products due to undeclared milk.

Class IHigh

FDAJul 6, 2012Nationwide• Arctic Zero, Inc.