High Risk Recalls

Hi-Tech Pharmaceuticals Top Secret Nutrition Uric Control Recalled 85,950 Units in 2025 for Unproved

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

Hi-Tech Pharmaceuticals L-Glutamine Ultra Pure Powder Recall: 85,950 Units (2025)

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

Hi-Tech Pharmaceuticals Slimaglutide 85,950-Unit Recall for Unapproved Drug Claims (2025)

Unapproved Drug Claims and Misbranded.

SeaSpine Orthopedics Recalled 74 Reef TA Inserter Instruments for Reef Interbody System (2025)

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 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 Pine Bark Supplements Recalled for Unapproved Drug Claims and Misbranding (H

Unapproved Drug Claims and Misbranded.

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

Unapproved Drug Claims and Misbranded.

Boston Scientific NephroMax Kit Recall Covers 458 Units Over Foreign Material Migration Risk

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.

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

M.O.M Enterprises Recalls 85,248 Organic BABY Bedtime Drops Over Spoilage Risk (2025)

Potential for spoilage due to yeast contamination.

Boston Scientific Encore 26 Inflation Device Recalled Over Foreign Particle Contamination

Tandem Diabetes Care Recalls 122,958 t:slim X2 and Tandem Mobi Pumps Over Autobolus Risk (2025)

Hans Kissle Company Recalls 66 Units of Red Bliss Potato Salad for Undeclared Wheat (2025)

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