High Risk Recalls

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.

B. Braun 23,100 0.9% Sodium Chloride Injection Containers Recalled for Sterility Concerns (2025)

B. Braun Medical Inc. recalls 23,100 0.9% Sodium Chloride Injection L 8000 containers nationwide. The recall cites lack of assurance of sterility and potential fluid leakage at a weld site. Stop using immediately and consult a healthcare provider.

Hospira Sodium Bicarbonate Vial Recall for Sterility Concerns Affects 15,750 Vials

Lack of Assurance of Sterility.

AVID Medical JACK421-04 ENT PACK Recalled for Sterility Risk (2025)

AVID Medical recalled 57 JACK421-04 ENT PACK convenience kits nationwide in Florida. The open header bag seals could compromise sterility. Consumers should stop using the device and follow manufacturer instructions for recall resolution.

Wasatch Photonics Raman Spectrometers Recall Expanded for Laser Safety Risks (2025)

B. Braun Medical Lactated Ringers Injection Recall for Sterility Concerns Affecting 74,088 Units (US

Lack of Assurance of Sterility; potential for fluid leakage at one of the weld sites.

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.

Hospira Epinephrine Injection Vials Recalled for Lack of Sterility Assurance (2025)

Lack of Assurance of Sterility.

Beckman Coulter DxC 500i Clinical Analyzer Modules Recalled for Processing Delays (2025)