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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

426

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 121–140 of 4598 recalls

Desipramine Tablets 25mg (Heritage) – Impurity Concerns (2025)

CGMP Deviations: N-Nitroso Desipramine impurity exceeding the permissible acceptable daily intake level.

Class IIModerate

FDAOct 6, 2025Nationwide• Heritage Pharmaceuticals Inc

Desipramine Tablets 150mg (Heritage) – Impurity Concerns (2025)

CGMP Deviations: N-Nitroso Desipramine impurity exceeding the permissible acceptable daily intake level.

Class IIModerate

FDAOct 6, 2025Nationwide• Heritage Pharmaceuticals Inc

Desipramine Tablets 100mg (Heritage) – Impurity Concerns (2025)

CGMP Deviations: N-Nitroso Desipramine impurity exceeding the permissible acceptable daily intake level.

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Class II

Moderate

FDAOct 6, 2025Nationwide• Heritage Pharmaceuticals Inc

Desipramine Tablets 50mg (Heritage) – Impurity Concerns (2025)

CGMP Deviations: N-Nitroso Desipramine impurity exceeding the permissible acceptable daily intake level.

Class IIModerate

FDAOct 6, 2025Nationwide• Heritage Pharmaceuticals Inc

Coca-Cola Zero Sugar 12 oz (Coca-Cola Southwest) – Metal Contamination (2025)

Potential presence of foreign material (metal) in the product

Class IIModerate

FDAOct 3, 2025TX• COCACOLA SOUTHWEST BEVERAGES LLC

Sprite 12 oz (Coca-Cola Southwest) – Metal Contamination (2025)

Potential presence of foreign material (metal) in the product

Class IIModerate

FDAOct 3, 2025TX• COCACOLA SOUTHWEST BEVERAGES LLC

Coca-Cola 12 oz (Coca-Cola Southwest) – Metal Contamination (2025)

Potential presence of foreign material (metal) in the product

Class IIModerate

FDAOct 3, 2025TX• COCACOLA SOUTHWEST BEVERAGES LLC

Magseed Pro 7cm Marker (Endomagnetics) – fiber contamination (2025)

Potential for contamination with cotton fibers.

Moderate

FDAOct 1, 2025Nationwide• ENDOMAGNETICS LTD St. Johns Innovation Park Cowley Road Cambridge United Kingdom

MAS Omni CARDIO Controls (Microgenics) – variability issue (2025)

The firm received complaints from customers reporting vial-to-vial variability when using the control with high sensitivity Troponin I assays. This defect may lead to as delay in patient results for hs Troponin I assays.

Moderate

FDAOct 1, 2025Nationwide• Microgenics Corporation

ProxiDiagnost N90 (Philips) – carriage movement issue (2025)

Philips has identified that some ceiling suspension telescopic carriages manufactured from July 2024 through June 2025 may be difficult to move vertically (i.e. additional force/physical exertion required for manual movement) due to potential manufacturing issues.

Moderate

FDAOct 1, 2025Nationwide• Philips Medical Systems DMC GmbH Development And Manufacturing Ctr. Rontgenstr. 24 Hamburg Germany

CombiDiagnost R90 (Philips) – carriage movement issue (2025)

Moderate

FDAOct 1, 2025Nationwide• Philips Medical Systems DMC GmbH Development And Manufacturing Ctr. Rontgenstr. 24 Hamburg Germany

DigitalDiagnost 4 (Philips) – carriage movement issue (2025)

Moderate

FDAOct 1, 2025Nationwide• Philips Medical Systems DMC GmbH Development And Manufacturing Ctr. Rontgenstr. 24 Hamburg Germany

Magseed Pro 12cm Marker (Endomagnetics) – fiber contamination (2025)

Potential for contamination with cotton fibers.

Moderate

FDAOct 1, 2025Nationwide• ENDOMAGNETICS LTD St. Johns Innovation Park Cowley Road Cambridge United Kingdom

Product may be contaminated with Listeria monocytogenes.

Class IHigh

FDASep 29, 2025NY• New Age International, Inc.

Carescape B450 Monitor (GE) – battery performance (2025)

Potential loss of monitoring on affected monitors when powered by certain batteries. Affected batteries can lose capability to hold charge and provide back up power. If this situation occurs, it will cause loss of patient monitoring and potentially delay recognizing patient status changes requiring treatment.

Moderate

FDASep 26, 2025Nationwide• GE Healthcare Finland Oy Kuortaneenkatu 2 Helsinki Finland