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Hi-Tech Pharmaceuticals Inc.

Hi-Tech Pharmaceuticals Inc. Recalls

All product recalls associated with Hi-Tech Pharmaceuticals Inc..

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Recall Summary

Total Recalls

1000

Past Year

899

Class I (Serious)

125

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 321–340 of 17592 recalls

Joint Health Supplement (iFORCE Nutrition) – Unapproved Claims (2025)

Unapproved Drug Claims.

Class IIILow

FDAAug 6, 2025AL, AZ, AR +46 more• Hi-Tech Pharmaceuticals Inc.

CADD Medication Cassette (ICU Medical) – bag weld issue (2025)

Certain CADD 50 mL and 100 mL Medication Cassette Reservoirs may exhibit weakened medication bag welds along the bag perimeter inside the plastic housing. This could result in medication leakage along the bag perimeter.

Moderate

FDAAug 6, 2025Nationwide• ICU Medical Inc.

Fish Oil Heart & Brain Supplement (Hi-Tech Pharmaceuticals) – Unapproved Claims (2025)

Unapproved Drug Claims.

Class IIILow

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Page 17 of 880Next

FDA

Aug 6, 2025

AL, AZ, AR +46 more

• Hi-Tech Pharmaceuticals Inc.

Adderex XR (Hi-Tech Pharmaceuticals) – Unapproved Claims (2025)

Unapproved Drug Claims and Misbranded.

Class IIILow

FDAAug 6, 2025AL, AZ, AR +46 more• Hi-Tech Pharmaceuticals Inc.

Beta Sitosterol (Hi-Tech Pharmaceuticals) – Unapproved Claims (2025)

Unapproved Drug Claims and Misbranded.

Class IIILow

FDAAug 6, 2025AL, AZ, AR +46 more• Hi-Tech Pharmaceuticals Inc.

Slimaglutide Weight Loss Aid (Hi-Tech Pharmaceuticals) – Misbranded Product (2025)

Unapproved Drug Claims and Misbranded.

Class IIILow

FDAAug 6, 2025AL, AZ, AR +46 more• Hi-Tech Pharmaceuticals Inc.

Uric Control (Top Secret Nutrition) – Unapproved Claims (2025)

Unapproved Drug Claims.

Class IIILow

FDAAug 6, 2025AL, AZ, AR +46 more• Hi-Tech Pharmaceuticals Inc.

Phytoform Fruits & Greens (Hi-Tech Pharmaceuticals) – Unapproved Claims (2025)

Unapproved Drug Claims and Misbranded.

Class IIILow

FDAAug 6, 2025AL, AZ, AR +46 more• Hi-Tech Pharmaceuticals Inc.

Phytoform Fruits & Greens (Hi-Tech Pharmaceuticals) – Unapproved Claims (2025)

Unapproved Drug Claims and Misbranded.

Class IIILow

FDAAug 6, 2025AL, AZ, AR +46 more• Hi-Tech Pharmaceuticals Inc.

Pinnacle Radiation Therapy System (Philips) – image error (2025)

Due to a software issue, there is a potential image error of the Region of Interest for expansion/contraction for HFP (Head First Prone), FFS (Feet First Supine) and FFP (Feet First Prone) orientations.

Moderate

FDAAug 5, 2025Nationwide• Philips Medical Systems (Cleveland) Inc

DxC 500 Analyzer (Beckman Coulter) – test processing issue (2025)

On a clinical analyzer, when ordering a Clinical Chemistry (CC) combination test simultaneously with an Immunoassay (IA) test, if the IA test is processed between the CC tests, CC sample status will remain In Progress with no errors, may cause processing delays.

Moderate

FDAAug 4, 2025Nationwide• Beckman Coulter Inc.

PhD Hemostasis Valve (Merit Medical) – manufacturing defect (2025)

Hemostasis valve has a manufacturing defect and when used the valve cap may remain depressed, leading to potential leakage, which may result in procedure inconvenience and/or hemorrhage.

Moderate

FDAAug 4, 2025AL, AK, AZ +47 more• Merit Medical Systems, Inc.

Potato Salad (Hans Kissle) – Undeclared Wheat (2025)

Undeclared Gluten

Contains undeclared wheat. The top label identifies the product as potato salad, but the unit contains pasta salad.

Class IIModerate

FDAAug 4, 2025CT, MA, NJ +2 more• Hans Kissle Company, LLC

Azurion System (Philips) – power supply issue (2025)

Philips Azurion and Allura systems configured with a 1 Phase Uninterruptible Power Supply (UPS) have the potential of shutting down and/or not starting up, if power to the system is lost.

Moderate

FDAAug 1, 2025Nationwide• PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. Veenpluis 4-6 Best Netherlands

Allura Xper X-Ray System (Philips) – component missing (2025)

Potential that a component (air baffle) may be missing in some Nehalem FlexVision-2 PCs that are part of the Allura Xper series.

Low

FDAAug 1, 2025Nationwide• PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. Veenpluis 4-6 Best Netherlands

Allura System (Philips) – power supply issue (2025)

Philips Azurion and Allura systems configured with a 1 Phase Uninterruptible Power Supply (UPS) have the potential of shutting down and/or not starting up, if power to the system is lost.

Moderate

FDAAug 1, 2025Nationwide• PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. Veenpluis 4-6 Best Netherlands

7up Zero Sugar Tropical Soda (Buffalo Rock) – mislabeled product (2025)

Product mislabeled - cans are labeled as Zero Sugar, but contain full sugar product

Class IIModerate

FDAJul 31, 2025AL, FL, GA• Buffalo Rock Company Inc

LinkSymphoKnee System (Waldemar Link) – screw issue (2025)

Some modular LinkSymphoKnee TiNbN Tibial Components were manufactured with two uncoated security screws, which is incorrect.

Low

FDAJul 31, 2025Nationwide• Waldemar Link GmbH & Co. KG (Mfg Site) Oststr. 4-10 Norderstedt Germany

Clearview Strep A Kit (Mckesson) – classification error (2025)

Due to a classification error in the inventory management system, specific medical devices were shipped to customers that did not have the requisite license to purchase such devices.

Low

FDAJul 30, 2025Nationwide• Mckesson Medical-Surgical Inc. Corporate Office 9954 Maryland Drive Deep Run Iii Ste. 4000 Richmond VA 23233

Epikut Plus Dental Implant (S.I.N. Implant) – storage conditions (2025)

Dental implants were imported under temperature and storage conditions that do not comply with the instructions for use and product labeling so there may be packaging damage, which could compromise product quality and performance.

Moderate

FDAJul 30, 2025Nationwide• S.I.N. Implant System Ltda Rua Soldador Ocimar Guimaraes da Silva 421 Jardim Analia Franco Sao Paulo Brazil