Regulatory Updates
Sep 17, 2026•1 min read
Trinity Biotech Recalls Oxalate Reagent B Lot 2500711 – Health Canada
Trinity Biotech is recalling Oxalate Reagent B (Product Code 591-2, Lot 2500711) due to performance variability that may produce falsely low oxalate results. Users should stop use and quarantine inventory.
Regulatory Updates
Sep 16, 2026•1 min read
Recall: Platinum Naturals Easymulti Stress (Men) Vitamin B6 Mislabel
Health Canada has recalled Platinum Naturals Easymulti Stress (Men) capsules (lots 737‑737C) due to incorrect Vitamin B6 labeling. Retailers should remove affected products.
Regulatory Updates
Sep 15, 2026•1 min read
Health Canada Issues Recall for Organika Lion's Mane, Reishi and Creatine Gummies
Health Canada has recalled three Organika gummy supplements after discovering they were imported from a foreign manufacturing site not listed on the site licence.
Regulatory Updates
Sep 12, 2026•1 min read
Yuyu Pharmaceutical receives 15‑day manufacturing suspension after premature re‑release of recalled products
Yuyu Pharmaceutical re‑shipped four voluntarily recalled items, including Tanamin tablets, before official recall closure, prompting the MFDS to impose a 15‑day manufacturing halt. The action was due to procedural lapses, not product safety.
Regulatory Updates
Sep 10, 2026•1 min read
Teva Canada Recalls Novo‑Gesic Forte 500 mg Acetaminophen Over Potential Foreign Material
Teva Canada is recalling a lot of Novo‑Gesic Forte 500 mg acetaminophen tablets due to possible phenolic resin or epoxy contamination that could injure the digestive system.
Regulatory Updates
Sep 10, 2026•1 min read
GE Healthcare alerts on two potential issues in Centricity High Acuity systems
GE Healthcare reports two potential safety issues affecting order and recording summary components in certain Centricity High Acuity systems.
Regulatory Updates
Sep 10, 2026•1 min read
Stryker Issues Labeling Alert for T2 Alpha IMN Advanced Locking Screw Lot
Stryker reports a labeling error in one lot of T2 Alpha IMN advanced locking screws, which contain 75 mm screws instead of the specified 57.5 mm.
Regulatory Updates
Sep 9, 2026•1 min read
Philips MR Imaging Systems Software Issue May Halt Exams
Philips reports a software fault in MR systems (versions R5 & R11) that can freeze the system during image reconstruction, requiring a restart.
Regulatory Updates
Sep 4, 2026•1 min read
Stryker LifePak R-35 Monitor-Defibrillator May Have Improperly Seated Connectors
Stryker discovered that some LifePak R-35 units may have printer and modem access port connectors not fully seated, potentially appearing flush or recessed.
Regulatory Updates
Sep 4, 2026•1 min read
Boston Scientific Initiates Recall of Imager II Angiographic Catheters Over Tip Issue
Boston Scientific is recalling Imager II Angiographic Catheters after discovering reduced stabilizing agents in the tip, which may increase risk of tip degradation and detachment.
Regulatory Updates
Sep 4, 2026•1 min read
Boston Scientific Initiates Recall of Imager II Angiographic Catheters
Boston Scientific is recalling Imager II catheters due to reduced stabilizing agents in the tip, which may increase risk of tip degradation and detachment.
Regulatory Updates
Sep 3, 2026•1 min read
Balt Extrusion Recalls ANRYV Connectors Over Endotoxin Test Issue
Balt Extrusion is voluntarily recalling certain ANRYV connector lots after bacterial endotoxin test failures; no patient harm reported.