Stay Informed

Get email alerts when new recalls match your interests.

Recall data is updated hourly from official government sources. Very recent recalls may not yet appear. About our data sources

About

We make U.S. recall data searchable and accessible for consumers and businesses.

Site

FAQ
Browse by State
Statistics
Recall Classifications
About
Enterprise API

Legal

Privacy Policy
Terms of Service
Report Incorrect Info

Official Sources

FDA Recalls ↗
USDA FSIS ↗
CPSC Recalls ↗
NHTSA Recalls ↗

RSS Feed

Home
/
Brands
/
Breckenridge Pharmaceutical, Inc

Breckenridge Pharmaceutical, Inc Recalls

All product recalls associated with Breckenridge Pharmaceutical, Inc.

Get alerts for this brand

Recall Summary

Total Recalls

1000

Past Year

1000

Class I (Serious)

127

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 1021–1040 of 25000 recalls

Duloxetine Capsules (Breckenridge) – Nitrosamine Impurity (2025)

CGMP Deviations: Presence of Nitrosamine Drug Substance Related Impurity above the proposed interim limit.

Class IIModerate

FDAApr 14, 2025Nationwide• Breckenridge Pharmaceutical, Inc

ChlorproMAZINE Tablets (Harvard Drug) – Nitrosamine Impurity (2025)

CGMP deviations: presence of N-Nitroso-Desmethyl Chlorpromazine impurity above the recommended interim limit

Class IIModerate

FDAApr 14, 2025Nationwide• The Harvard Drug Group LLC dba Major Pharmaceuticals and Rugby Laboratories

Duloxetine Capsules (Breckenridge) – Nitrosamine Impurity (2025)

CGMP Deviations: Presence of Nitrosamine Drug Substance Related Impurity above the proposed interim limit.

1...50 515253 54...1250

Page 52 of 1250Next

Class IIModerate

FDAApr 14, 2025Nationwide• Breckenridge Pharmaceutical, Inc

ZF North America Brake Chamber (ZF) – Brake Replacement (2025)

Fire/Burn Risk

Nova Bus (US) Inc. (Nova Bus) is recalling certain ZF North America Knorr-Bresme 20/22-57 brake chambers, with part number K038830N00, sold as replacement parts for certain buses. The brake chamber may have been improperly manufactured, which can result in an air leak.

High

NHTSAApr 14, 2025Nationwide• ZF NORTH AMERICA

Cilantro Salsa (MegaMex Foods) – foreign wood pieces (2025)

Firm's salsa product was potentially manufactured with a recalled ingredient (Fresh Cilantro containing foreign objects "wood pieces")

Class IIModerate

FDAApr 14, 2025CA, IN, MI +3 more• MegaMex Foods LLC

Coachmen Catalina (Coachmen) – Tank Pipe Issue (2025)

Forest River, Inc. (Forest River) is recalling certain Coachmen Catalina BCAT154RBX travel trailers. The wastewater holding tank pipe may not extend to the exterior of the vehicle, allowing sewer gas to enter the cabin.

Moderate

NHTSAApr 10, 2025Nationwide• COACHMEN

RAM 1500 (RAM) – Tire Pressure Warning (2025)

Chrysler (FCA US, LLC) is recalling certain 2025 Ram 1500 vehicles. A software error may cause an incorrect tire inflation pressure message to display on the instrument panel.

Moderate

NHTSAApr 10, 2025Nationwide• RAM

Blueprint Software (Tornier) – Case Access Issue (2025)

A software bug in Blueprint version 4.2.1 prevents users from accessing cases initiated in previous versions of the software.

Moderate

FDAApr 10, 2025Nationwide• Tornier S.A.S. 161 Rue Lavoisier Montbonnot-Saint-Martin France

Coachmen Brookstone (Coachmen) – Tank Pipe Issue (2025)

Forest River, Inc. (Forest River) is recalling certain 2025 Coachmen Brookstone BKF398MBL fifth wheels. The wastewater holding tank pipe may not extend to the exterior of the vehicle, allowing sewer gas to enter the cabin.

Moderate

NHTSAApr 10, 2025Nationwide• COACHMEN

AirLife Infant Circuit (Vyaire) – Adapter Disconnect (2025)

Adapters may disconnect during setup or while in use, potentially interrupting ventilation. Any disconnection can result in severe consequences for neonates, including hypoxia, hypercapnia, and organ failure.

Moderate

FDAApr 10, 2025Nationwide• Vyaire Medical

ClomiPRAMINE Hydrochloride Capsules (Lupin) – Impurity Specification Failure (2025)

Failed Impurities/Degradation Specifications: an out of specification result observed in degradation product test (any unspecified degradation product) during 18-month long term stability study.

Class IIModerate

FDAApr 10, 2025Nationwide• Lupin Pharmaceuticals Inc.

CMS8000 Patient Monitor (Contec) – Cybersecurity Risk (2025)

Patient monitor has nine identified cybersecurity vulnerabilities.

Moderate

FDAApr 10, 2025Nationwide• Contec Medical Systems Co., Ltd. Economic And No.

FoundationOne Diagnostic (Foundation Medicine) – Variant Reporting (2025)

Four (4) total reports were sent to customers with clinically relevant variants requiring amendment, one (1) of which with an incorrect negative CDx claim. The remaining three (3) with tumor profiling result changes did not impact CDx indications.

Moderate

FDAApr 9, 2025Nationwide• Foundation Medicine, Inc.

Hemopropin Ointment (Apipharma) – CGMP Deviations (2025)

CGMP Deviations

Class IIModerate

FDAApr 9, 2025AZ• Apipharma

Kapsin Ointment (Apipharma) – CGMP Deviations (2025)

CGMP Deviations

Class IIModerate

FDAApr 9, 2025AZ• Apipharma

PiezoWave 2 Control Unit (Richard Wolf) – Capacitor Failure (2025)

Fire/Burn Risk

The high voltage capacitor may fail early in the product life cycle after delivery of surge voltages. When this failure occurs, the capacitor may produce smoke and a burning smell. In extremely rare instances a capacitor may cause a spark or excessive heat when an internal capacitor failure occurs.

High

FDAApr 9, 2025GA• Richard Wolf GmbH Pforzheimer Str. 32 Knittlingen Germany

Artix MT Thrombectomy Device (Inari) – Vessel Range (2025)

Thrombectomy device specifies vessel range of 2.5-6 mm on the pouch, carton, and Instructions for Use rather than the correct vessel range of 3-6 mm, which could incrementally increase the radial force on the artery, which has the potential of vascular complications.

Low

FDAApr 8, 2025Nationwide• Inari Medical Oak Canyon

Ambu aScope 5 Broncho (Ambu) – Incorrect Labeling (2025)

Incorrect labeling in which the front red pouch label did not match the actual size of the medical device. The label on the front of the scope incorrectly states 5.0/2.2 while the back label, shipping box and product inside correctly states 5.6/2.8.

Low

FDAApr 7, 2025Nationwide• Ambu Inc.

Bio 1 Granules (Science & Bio Materials) – Insufficient Product Volume (2025)

Vials of implant bone granules may contain less product then specified on labeling.

Low

FDAApr 7, 2025Nationwide• SCIENCE & BIO MATERIALS Zi Du Monge Lourdes France

Microstream Advance CO2 Filter (Philips) – Adapter Disconnection Risk (2025)

Disconnection of the adapter from the endotracheal tube can potentially be difficult or not possible.

Moderate

FDAApr 7, 2025Nationwide• Philips North America Llc