Read the latest recall alerts from various industries. Stay informed and stay safe.
# Major Recall Alert: IceSeed 1.5 CX 90 Needle Recalled Due to Programming Issue Boston Scientific has recently issued an advisory regarding its **I...
Read More# Major Recall Alert: Monkfish Liver Recalled Due to Potential or Undeclared Allergen - Milk Food safety alert! JJWV Marketing Corporation, based i...
Read More# Major Recall Alert: REMISOL Advance Error with Patient DOB Misinterpretation Prompts Urgent Action Beckman Coulter has issued a significant recal...
Read More# Major Recall Alert: Male Enhancement Dietary Supplements Recalled Due to Undeclared Chloropretadalafil, Propoxyphenylsildenafil, Sildenafil On Ap...
Read More# Major Recall Alert: Happy Easter White Rabbit Hoodie Recalled Due to Fire Hazard Label Non-Compliance Attention parents and guardians in Australi...
Read More# Major Recall Alert: SHEIN Children’s Pyjama Sets Recalled Over Safety Concerns SHEIN has announced an urgent product recall for its *Two piece ...
Read More# Major Recall Alert: CADD-Solis VIP™ Ambulatory Infusion Pump and CADD-Solis™ Ambulatory Infusion Pump Recalled Due to Serious Battery-Related Is...
Read More# Major Recall Alert: Chlorpromazine Hydrochloride Tablets, USP 10 mg, 100’s Count, Gabapentin Capsules, Propafenone Hydrochloride ER Capsules, Soli...
Read More# Major Recall Alert: Sesame Miso Salad with Salmon Recalled Due to Potential or Undeclared Allergen - Milk Trader Joe’s Sesame Miso Salad with S...
Read More# Major Recall Alert: KickAss Rechargeable Head Torch (Model: KAHEADTORCH) Recalled Due to Overheating Risk Consumers in Australia, take note! KickAs...
Read More# Major Recall Alert: Spicy Chicken Nacho Soup and Wicked Thai Style Soup Recalled Due to Pieces of Wood Campbell’s has announced a significant rec...
Read More# Major Recall Alert: CADD-Solis VIP™ and CADD-Solis™ Ambulatory Infusion Pumps Recalled Due to False Upstream Occlusion (USO) Alarms On April ...
Read More# Major Recall Alert: Hemospray® Kit Recalled Due to Activation Knob Safety Issue On November 4, 2024, an important recall was issued for certain ...
Read More# Major Recall Alert: PMS-FLUOXETINE 10mg, PMS-FLUOXETINE 20mg Recalled Due to Exceeding Interim Acceptable Limit for N-nitroso-fluoxetine In an impo...
Read More# Major Recall Alert: FRED Easyport Recalled Due to Defective IGBT Modules, Effective April 1, 2025 Schiller Ag, a trusted name in medical equipment,...
Read More# Major Recall Alert: Pacemaker Packs Recalled Due to Surgical Needle Coating Defect *Recall Start Date: April 7, 2025* If you’ve recently used o...
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