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Rising Pharma Holding, Inc.

Rising Pharma Holding, Inc. Recalls

All product recalls associated with Rising Pharma Holding, Inc..

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Recall Summary

Total Recalls

1000

Past Year

631

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 521–540 of 10391 recalls

Duloxetine Capsules (Rising Pharma) – Nitrosamine Impurity (2025)

CGMP Deviations: Presence of N-nitroso-duloxetine impurity above recommended interim limit.

Class IIModerate

FDAMar 5, 2025Nationwide• Rising Pharma Holding, Inc.

Panang Curry Tofu (Seattle Homemade Thai) – undeclared soy (2025)

Label declares tofu but it does not declare soy.

Class IIModerate

FDAMar 4, 2025IN, WA• Seattle Homemade Thai LLC

Tolterodine Tartrate (Major Pharmaceuticals) – Dissolution Failure (2025)

Failed Dissolution Specifications: Out of specification results obtained during routine stability testing for dissolution.

Class III

1...25 262728 29...520

Page 27 of 520Next

Low

FDAMar 4, 2025Nationwide• The Harvard Drug Group LLC dba Major Pharmaceuticals and Rugby Laboratories

NovumIQ Syringe Infusion System (Baxter) – Incorrect Installation (2025)

Baxter Healthcare Corporation is issuing an Urgent Medical Device Recall for the Novum IQ syringe pumps listed below due to an incorrectly installed gasket. A gasket failure could lead to potential fluid ingress due to cleaning, or as a result of an IV fluid spill.

High

FDAMar 3, 2025Nationwide• Baxter Healthcare Corporation

TRUBLUE iQ Auto Belays (Head Rush Technologies) – fall hazard (2025)

This recall involves TRUBLUE iQ Auto Belay Devices, which enable climbers to safely descend while climbing. The TRUBLUE iQ is gray with blue handles and a gray sash on the front cover. The TRUBLUE iQ+ has an added catch-and-hold brake on the front. The LT versions of the iQ and iQ+ have blue tags above the blue webbing hand grip; the XL versions have a purple tag. The recalled auto belay devices have a serial number within the following serial number ranges printed on the device's handle, as well on the bottom of the device: Products Models Serial Number Range TRUBLUE iQ LT TBiQ LT (12.5m) iQ0041591 through iQ0044486 TRUBLUE iQ+LT TBiQ+ LT (12.5m) iQP000401 through iQP000422 TRUBLUE iQ XL TBiQ XL (20m) iQXL01283 through iQXL03425 TRUBLUE iQ+XL TBiQ+ XL (20m) iQXLP0104 through iQXLP0215

Very High

CPSCFeb 27, 2025Nationwide• Head Rush Technologies, of Louisville, Colorado

TS7500 MOBIUS Operating Table (Baxter) – Software Control Fault (2025)

There is a software issue which causes the upper back section to not be operable/adjustable when the "emergency mode" function is enabled.

Moderate

FDAFeb 25, 2025Nationwide• Baxter Healthcare Corporation

Zenition 70 (Philips) – Radiation Emission Risk (2025)

A wireless foot switch pedal may get stuck in the active position when the user releases the pedal, resulting in the emission of unintended radiation.

High

FDAFeb 25, 2025Nationwide• Philips North America Llc

TruSystem 7500 (Baxter) – Software Control Fault (2025)

There is a software issue which causes the upper back section to not be operable/adjustable when the "emergency mode" function is enabled.

Moderate

FDAFeb 25, 2025Nationwide• Baxter Healthcare Corporation

TruSystem 7500 Mobile Column (Baxter) – Software Control Fault (2025)

There is a software issue which causes the upper back section to not be operable/adjustable when the "emergency mode" function is enabled.

Moderate

FDAFeb 25, 2025Nationwide• Baxter Healthcare Corporation

Progressa Bed Surfaces (Baxter) – Air Bladder Movement (2025)

The air bladders inside the mattress may move out of position when the head of the bed is elevated, causing a dip in the mattress.

Moderate

FDAFeb 25, 2025Nationwide• Baxter Healthcare Corporation

TruSystem 7500 Hybrid (Baxter) – Software Control Fault (2025)

There is a software issue which causes the upper back section to not be operable/adjustable when the "emergency mode" function is enabled.

Moderate

FDAFeb 25, 2025Nationwide• Baxter Healthcare Corporation

Zenition 50 (Philips) – Radiation Emission Risk (2025)

A wireless foot switch pedal may get stuck in the active position when the user releases the pedal, resulting in the emission of unintended radiation.

High

FDAFeb 25, 2025Nationwide• Philips North America Llc

TruSystem 7500 Hybrid Plus (Baxter) – Software Control Fault (2025)

There is a software issue which causes the upper back section to not be operable/adjustable when the "emergency mode" function is enabled.

Moderate

FDAFeb 25, 2025Nationwide• Baxter Healthcare Corporation

Veradius Unity (Philips) – Radiation Emission Risk (2025)

A wireless foot switch pedal may get stuck in the active position when the user releases the pedal, resulting in the emission of unintended radiation.

High

FDAFeb 25, 2025Nationwide• Philips North America Llc