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Heritage Pharmaceuticals, Inc.

Heritage Pharmaceuticals, Inc. Recalls

All product recalls associated with Heritage Pharmaceuticals, Inc..

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Recall Summary

Total Recalls

1000

Past Year

422

Class I (Serious)

Most Recent

Jan 2026

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 2101–2120 of 4598 recalls

Losartan Potassium 100mg Tablets (Heritage) – Impurity Detection (2019)

CGMP Deviations: FDA lab confirmed presence of an impurity, N-Methylnitrosobutyric acid (NMBA) in the finished product above the interim acceptable daily intake level at the manufacturer

Class IIModerate

FDAMay 3, 2019Nationwide• Heritage Pharmaceuticals, Inc.

Losartan Potassium 50mg Tablets (Heritage) – Impurity Detection (2019)

CGMP Deviations: FDA lab confirmed presence of an impurity, N-Methylnitrosobutyric acid (NMBA) in the finished product above the interim acceptable daily intake level at the manufacturer

Class IIModerate

FDAMay 3, 2019Nationwide• Heritage Pharmaceuticals, Inc.

Dole Classic Coleslaw (Dole Vegetables) – Soft Plastic Pieces (2019)

1...104 105106107 108...230

Page 106 of 230Next

Complaints received of irregular pieces of soft plastic in the product.

Class IIModerate

FDAMay 2, 2019AL, AZ, CA +28 more• Dole Fresh Vegetables

Dole Colourful Coleslaw (Dole Vegetables) – Soft Plastic Pieces (2019)

Complaints received of irregular pieces of soft plastic in the product.

Class IIModerate

FDAMay 2, 2019AL, AZ, CA +28 more• Dole Fresh Vegetables

First Street Dark Chocolate Nonpareils (Heritage Candy) – Almond Mix-up (2019)

Customer discovered that some bags of dark chocolate non pareils contain dark chocolate almonds.

Class IIModerate

FDAMay 1, 2019AZ, CA, NV• Heritage Candy Company

Ketorolac Injection (Sagent Pharmaceuticals) – Microbial Growth (2019)

Lack of Sterility Assurance: Microbial growth detected during a routine simulation of the manufacturing process, which represents the potential introduction of microorganisms into the products.

Class IIModerate

FDAApr 30, 2019Nationwide• Sagent Pharmaceuticals Inc

Cytocell Ltd. 418 Cambridge Science Park, Milton Road Oxford Gene Technology Cambridge United Kingdom: Aquarius D13S319 Plus Deletion Probe, Model LPH068-A P...

There is an error in the chromomap on the package insert.

FDAApr 26, 2019Nationwide• Cytocell Ltd. 418 Cambridge Science Park, Milton Road Oxford Gene Technology Cambridge United Kingdom

Vitodens Boilers (Viessmann) – carbon monoxide hazard (2019)

This recall involves the Vitodens 200-W and Vitodens 222-F series boilers used for space or domestic water heating. There are five affected models in a specific serial number range. The Vitodens 200-W is a wall hung unit, housed in a white metal box about 38 inches high and 18 inches wide. The Vitodens 222-F is a floor mounted unit, housed in a white metal box about 68 inches tall and 24 inches wide. The name "Vitodens" is printed on the label on the outside of the boiler box. The product name and model number can be found on the left side of the boiler cover. The serial number can be found on the underside of the wall mounted boiler and on the center section on the floor mount model. Product Model Part Number Serial Number Range Vitodens 200-W B2HB 19 7538092 7538092401003107 to 7538092701038106 B2HB 26 7538093 7538093401002107 to 7538093701177109 B2HB 35 7538094 7538094401003101 to 7538094701446103 Vitodens 222-F B2TB 19 7542250 7542250401001100 to 7542250401210106 B2TB 35 7542251 7542251401001107 to 7542251701257105

CPSCApr 25, 2019Nationwide• Viessmann Werke GmbH & Co KG, of Germany

Fentanyl Transdermal System (Alvogen) – Product Mix-Up (2019)

Product Mix-Up: Customer complaint that their carton labeled as Fentanyl Transdermal Systems, 12 mcg/h contained five patches labeled and containing 50 mcg/h.

Class IHigh

FDAApr 19, 2019Nationwide• Alvogen, Inc

Malibu Black Vanilla Ice Cream (Le Cafe) – plastic pieces (2019)

Firm has received two complaints of plastic pieces in ice cream.

Class IIModerate

FDAApr 15, 2019CA• LE CAFE DE LA PLAGE

2012 DODGE DART Recall: POWER TRAIN:AUTOMATIC TRANSMISSION:LEVER AND LINKAGE:FLOOR SHIFT

Chrysler (FCA US LLC) is recalling certain 2013-2016 Dodge Dart vehicles equipped with 6-speed automatic transmissions. The shifter cable bushing may fail allowing the shift cable to detach from the transmission.

NHTSAApr 11, 2019Nationwide• DODGE

2016 NORTH CENTRAL EMERGENCY FORD E-350 Recall: EXTERIOR LIGHTING:BRAKE LIGHTS

North Central Emergency Vehicles (North Central) is recalling certain 2016-2018 Ambulances remounted on Ford E-350 and E-450 and Chevrolet G4500 chassis equipped with Whelen brake lights. Depending on the specific wiring of the vehicle, these brake lights may illuminate when the brake pedal has not been pressed.

NHTSAApr 10, 2019Nationwide• NORTH CENTRAL EMERGENCY

L'Explorateur Cheese (Societe Fromagere de la Brie) – Listeria Risk (2019)

Listeria

The product may be contaminated with Listeria monocytogenes.

Class IHigh

FDAApr 10, 2019IN• Societe Fromagere de la Brie

Brie Cheese (Fromagere de la Brie) – Listeria Risk (2019)

Listeria

The product may be contaminated with Listeria monocytogenes.

Class IHigh

FDAApr 10, 2019IN• Societe Fromagere de la Brie

Clonidine HCL Injection (X-Gen) – Labeling Error (2019)

Labeling: Label Error on Declared Strength: Side carton panel incorrectly lists the concentration as "500 mcg Clonidine Hydrochloride" rather than the correct concentration of "100 mcg Clonidine Hydrochloride" per mL.

Class IIILow

FDAMar 29, 2019Nationwide• X-Gen Pharmaceuticals Inc.

2019 DODGE CHARGER Recall: AIR BAGS

Chrysler (FCA US LLC) is recalling certain 2019 Dodge Charger vehicles. The driver and passenger sun visors may lack the required air bag warning information. As such, these vehicles fail to comply with Federal Motor Vehicle Safety Standard (FMVSS) number 208, "Occupant Crash Protection."

NHTSAMar 28, 2019Nationwide• DODGE

2019 GENIE TZ-34 Recall: ELECTRICAL SYSTEM:12V/24V/48V BATTERY:CABLES

Fire/Burn Risk

Genie Industries, Inc. (Genie) is recalling certain 2019 TZ-34 and TZ-50 trailer-mounted aerial devices. The battery cable ends at the quick disconnect may have been improperly crimped, resulting in possible excessive heat build-up of the conductor.

NHTSAMar 28, 2019Nationwide• GENIE

2019 VOLKSWAGEN TIGUAN Recall: EQUIPMENT:OTHER:LABELS

Volkswagen Group of America, Inc. (Volkswagen) is recalling certain 2019 Tiguan LWB vehicles. The tire information label contains inaccurate tire dimension and inflation pressure specifications. As such, these vehicles fail to comply with the requirements of Federal Motor Vehicle Safety Standard (FMVSS) number 110, "Tire Selection and Rims."

NHTSAMar 27, 2019Nationwide• VOLKSWAGEN

Home Elevators (Cambridge Elevating) – fall risk (2019)

This recall involves Cambridge Elevating Elmira, Heritage & Hybrid model home elevators using the first and second generation micro-controller systems (BES 1 & BES 2). "Cambridge Elevating" is printed on the label inside the elevators. The elevators have an operating panel inside the cab with a digital display, a stop button, the elevator capacity and a phone box. Only elevators with production date codes 1/2/2009 through 29/11/17 printed on the manufacture label inside the elevator wall are included in the recall.

CPSCMar 27, 2019Nationwide• Cambridge Elevating, of Cambridge, Ontario Canada

Thallous Chloride Injection (GE Healthcare) – Chemical Contamination (2019)

Chemical Contamination: Trace amounts of an impurity was detected in the reagent used to manufacture finished product.

Class IIILow

FDAMar 26, 2019Nationwide• Medi-Physics Inc. dba GE Healthcare