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Bryant Ranch Prepack, Inc. dba BRP Pharmaceuticals

Bryant Ranch Prepack, Inc. dba BRP Pharmaceuticals Recalls

All product recalls associated with Bryant Ranch Prepack, Inc. dba BRP Pharmaceuticals.

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Recall Summary

Total Recalls

1000

Past Year

432

Class I (Serious)

138

Most Recent

Dec 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 2801–2820 of 7663 recalls

Spironolactone Tablets (Bryant Ranch) – Label Mix-Up (2021)

Labeling: Label Mix-Up - Prepackaged bottles labeled spironolactone 25 mg may contain spironolactone 50 mg tablets.

Class IHigh

FDAJan 27, 2021Nationwide• Bryant Ranch Prepack, Inc. dba BRP Pharmaceuticals

Digital X-ray Imaging System (Shanghai United) – X-Ray Motion Hazard (2021)

There is a potential for the X-Ray tube head (Touch screen interface) to perform an uncommanded motion. This could result in a collision with the patient.

FDAJan 25, 2021Nationwide• Shanghai United Imaging Healthcare Co., Ltd. No. 2258 Chengbei Rd, Jiading Ind. Shanghai China

Barco MDNC-3421 Display (Barco) – DICOM Non-Compliance (2021)

A number of MDNC-3421 displays were shipped while not being DICOM-compliant. These displays will not pass DICOM acceptance tests.

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FDAJan 22, 2021WI• Barco N.V. President Kennedypark 35 Kortrijk Belgium

Cephalexin Oral Suspension (Ascend) – Impurity Deviation (2021)

CGMP Deviations: Individual Unidentified impurities results of the product was found at higher side of the specification limit.

Class IIModerate

FDAJan 22, 2021Nationwide• Ascend Laboratories LLC

Cephalexin Oral Suspension (Ascend) – Impurity Deviation (2021)

CGMP Deviations: Individual Unidentified impurities results of the product was found at higher side of the specification limit.

Class IIModerate

FDAJan 22, 2021Nationwide• Ascend Laboratories LLC

CervAlign Cervical Plate (RTI Surgical) – Locking Mechanism Failure (2021)

Locking mechanism has been observed to disassociate either intraoperatively or postoperatively resulting in replacement/revision

FDAJan 15, 2021Nationwide• RTI Surgical, Inc. (dba Pioneer Surgical Technology, Inc.)

CT Port Insertion Kit (MedComp) - Incorrect Port Size (2021)

The 5F Dignity CT Port kits were packaged with the incorrect size port. The kits include a 6.6F port instead of the correct 5F port. The inability to connect the catheter lumen to the port stem because of the incorrect size may not be noted until well into the procedure, after the catheter lumen is placed in the vessel. An alternate port will need to be obtained prolonging the procedure. A prolonged insertion procedure increases any risk associated with a surgical procedure.

FDAJan 13, 2021Nationwide• Medical Components, Inc dba MedComp

Natus EDS CSF Drainage (Natus) - Pyrogen Test Failure (2021)

The external drainage system failed to meet Pyrogen test requirements for devices contacting cerebrospinal fluid of 2.15 endotoxins.

FDAJan 12, 2021Nationwide• Natus Manufacturing Limited Ida Business Park Glenbrack Road Galway Ireland

Bard Clean-Cath Catheter (Bard) - Packaging Integrity Issue (2021)

Laceration Risk

The device catheter tip was cut off (no tip) and the product packaging was not fully sealed.

FDAJan 11, 2021Nationwide• C.R. Bard, Inc.

Slush Warmer Disc Drape (Ecolab) - Manufacturing Defect (2021)

Slits were identified in a low quantity of ORS-320 Slush + Warmer Disc Drapes from a single lot. A source for potential manufacturing error was identified and investigation is underway to prevent further recurrence. The slits may lead to a breach in the sterile barrier between fluid in the basin and the slush/warming equipment. This could pose a risk of infection to patients receiving warmed irrigation fluid or surgical slush if used during a procedure.

FDAJan 11, 2021Nationwide• Ecolab Inc

Sulfur Ointment (DLC) – Label Mix-Up (2021)

Labeling: Label Mix-Up. THe English label with Drug Facts panel for Camphor was incorrectly placed on product.

Class IIModerate

FDAJan 6, 2021Nationwide• DLC Laboratories, Inc

HAMILTON-H900 Humidifier (Hamilton Medical) - Startup Malfunction (2021)

When starting a humidifier, intended for respiratory gas conditioning during invasive and noninvasive mechanical ventilation, with an empty chamber, and water is not filled into the chamber, the low water level alarm will be delayed and medical staff are unaware that there is no water in the chamber.

FDAJan 5, 2021CA, FL, NV +3 more• Hamilton Medical AG Via Crusch 8 Bonaduz Switzerland