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Preventics, Inc. dba Legere Pharmaceuticals

Preventics, Inc. dba Legere Pharmaceuticals Recalls

All product recalls associated with Preventics, Inc. dba Legere Pharmaceuticals.

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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 601–620 of 17592 recalls

Rodex Forte Supplement (Legere Pharmaceuticals) – undeclared colors (2025)

Undeclared Allergen

Undeclared Allura Red (Red No. 40) and Brillant Blue (Blue No.1) used in gelatin capsules.

Class IIILow

FDAApr 30, 2025Nationwide• Preventics, Inc. dba Legere Pharmaceuticals

Protrim Plus Supplement (Legere Pharmaceuticals) – undeclared colors (2025)

Undeclared Allergen

Undeclared Allura Red (Red No. 40) and Brillant Blue (Blue No.1) used in gelatin capsules.

Class IIILow

FDAApr 30, 2025Nationwide• Preventics, Inc. dba Legere Pharmaceuticals

H&C Farms Raw Tomatoes (Hanshaw & Capling) – salmonella risk (2025)

1...29 303132 33...880

Page 31 of 880Next

Salmonella

Potential Salmonella Contamination

Class IHigh

FDAApr 29, 2025FL, IL, IN +5 more• Hanshaw & Capling Farms, LLC

AcoSound Hearing Aid (AcoSound) – Labeling Error (2025)

Three issues 1. Label error: The manufacturer information in the labeling is not correct, the manufacturer's name is mislabeled as "Developed by AcoSound," Correct should be "Manufactured by Hangzhou AcoSound." And the labeling has no statement of the place of business for the manufacturer. 2. Customer information: The customer "Blaid" information is not correctly marked; Blaid is not the manufacturer. 3. UDI Information: The UDI information is incomplete and without DI information and correct Pl information, not complied with UDI label requirements.

Low

FDAApr 25, 2025Nationwide• HANGZHOU ACOSOUND TECHNOLOGY CO., LTD. No.2 Building Room 401 No.

15 Degree Stab Knife (Tecfen) – Sterility Assurance (2025)

Sterility assurance for Ophthalmic knives.

Moderate

FDAApr 25, 2025Nationwide• Tecfen Medical

Infuvite Adult Vitamins (Mckesson) – Cold Chain Transit Delay (2025)

Severe thunderstorms caused transit delays of certain cold chain products that were shipped on 02-Apr-2025 and delivered after the 48-hours specified delivery time, on 07-Apr-2025 and 08-Apr-2025. The affected products may not have been stored at the recommended labeled storage conditions which may have impacted the safety, quality, identity, potency and purity of the product.

Class IIModerate

FDAApr 25, 2025FL, IN, MS• Mckesson Medical-Surgical Inc. Corporate Office

Medroxyprogesterone Acetate Injection (Mckesson) – Cold Chain Transit Delay (2025)

Class IIModerate

FDAApr 25, 2025FL, IN, MS• Mckesson Medical-Surgical Inc. Corporate Office

MUSE 5 Systems (GE Medical) – Network Credential Risk (2025)

The MUSE Administrator Account active directory or local credential could potentially be used from your local network to log into a GE HealthCare MUSE 5 system and potentially manipulate recorded patient data.

High

FDAApr 25, 2025Nationwide• GE Medical Systems Information Technologies Inc

HemoClue Hemotrol Control (Mckesson) – Cold Chain Disruption (2025)

transit delays of certain cold chain products due to severe thunderstorms which may caused the products to be stored outside the recommended labeled storage conditions. This failure could increase the probability of an incorrect test result or a delayed test result.

Moderate

FDAApr 24, 2025Nationwide• Mckesson Medical-Surgical Inc. Corporate Office 9954 Maryland Drive Deep Run Iii Ste. 4000 Richmond VA 23233

Bombardier Recreational Products (BRP) is recalling certain 2025 Can-Am Origin and Pulse electric motorcycles. The breather valve may not seal properly and allow moisture or water to enter the high voltage battery.

High

NHTSAApr 24, 2025Nationwide• CAN-AM