cpsc regulated Recalls

Hi-Tech Pharmaceuticals Quercetin Dietary Supplement Recalled for Unapproved Drug Claims and Misbrnd

Unapproved Drug Claims and Misbranded.

Hi-Tech Pharmaceuticals iFORCE Joint Help Recall 85,950 Units for Unapproved Drug Claims (2025)

Hi-Tech Pharmaceuticals’ PrimeNutrition PhytoForm Fruits & Greens Recall for Unapproved Drug Claims

Unapproved Drug Claims and Misbranded.

Hi-Tech Pharmaceuticals Beta Sitosterol 715mg Recalled for Unapproved Claims (2025)

Unapproved Drug Claims and Misbranded.

Hi-Tech Pharmaceuticals PrimeNutrition Taurine Recall 85,950 Units in 2025

Unapproved Drug Claims and Misbranded.

Hi-Tech Pharmaceuticals Formutech Nutrition Joint Formula Recalled for Unapproved Drug Claims (2025)

Hi-Tech Pharmaceuticals Dietary Supplement LG Sciences Battle Hardener Platinum Series Recall for Un

Olympus ViziShot 2FLEX Biopsy Device Recalled for Deformed Tips in 103,731 Units

Potential for undetected, deformed a-traumatic tips.

Glenmark Carvedilol 25 mg Recall Expands Over NNCI Impurity Above FDA Limit in 14,976 Bottles

CGMP Deviations: Results for N-Nitroso Carvedilol Impurity-1 (NNCI) impurity observed to be above the FDA-recommended limit of NMT 4.0 ppm

Glenmark Carvedilol 12.5 mg Tablets Recalled for NNCI Impurity Exceeding FDA Limit (2025)

CGMP Deviations: Results for N-Nitroso Carvedilol Impurity-1 (NNCI) impurity observed to be above the FDA-recommended limit of NMT 4.0 ppm

Hi-Tech Pharmaceuticals Recalls PrimeNutrition PhytoForm Fruits & Greens Formula 30 Servings for Unf

Unapproved Drug Claims and Misbranded.

Maquet Vasoview Hemopro 3 EVH System Recall Affects 98 Units, 16 Complaints of Out-of-Box Failures

Maquet Cardiovascular recalled 98 Vasoview Hemopro 3 EVH systems nationwide across FL, IL, MD and TX after 16 out-of-box failure complaints. No serious injuries were reported. The failures occurred during limited launch before clinical use.

Hi-Tech Pharmaceuticals Adderex XR Recall 85,950 Units for Unapproved Claims (2025)

Unapproved Drug Claims and Misbranded.

Hi-Tech Pharmaceuticals Joint-RX Dietary Supplement Recalled for Unapproved Drug Claims (2025)

Sandoz/Cardinal Health Enoxaparin Sodium Injection Recall Over Mispacked Bags

Enoxaparin Sodium Injection recall active as of 2025. Cardinal Health and Sandoz Inc. distributed the product in Kansas. Bags labeled 80 mg/0.8 mL contained 30 mg/0.3 mL doses. Health authorities urge immediate stop-use and guidance from providers.

Haleon US Recall: Sensodyne PRONAMEL Active SHIELD Toothpaste Recalled for Label Mix-Up

Labeling: Label Mix-up: The outer carton is labelled Fresh Mint. The tube is labelled Cool Mint/Whitening. The toothpaste inside the tube is Fresh Mint as indicated on the outer carton

Boston Scientific UroMax Ultra Kit MPNs Recalled Over Foreign Material Migration Risk (2025)

Philips Pinnacle3 Recall: 810 Units Over ROI Image Error in 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.

Boston Scientific Encore 26 Inflation Device Recalled Over Foreign Particle Contamination

AVID Medical CPT BASIC IR PACK 1646381 Recall for Sterility Risk (2025)

AVID Medical recalls 228 CPT BASIC IR PACKs sold nationwide, including Florida, due to open header bag seals that may compromise sterility. The recall is active as of September 17, 2025. Consumers should stop use and follow manufacturer instructions.