HIGHFDA DEVICE
IntelliVue Patient Monitor MX700. Product Number: 865241.
Potential issue where the IntelliVue monitors did not alarm.
Philips North America
Potential issue
These recalls involve products that pose serious risks of injury or death. Check if you own any of these products and take immediate action if needed.
High Risk Recalls
2,324 critical product recalls that require immediate attention. These products have been identified as posing serious safety hazards.
What to do if you own a recalled product:
- Stop using the product immediately
- Keep the product away from children
- Follow the remedy instructions provided
- Contact the manufacturer for a refund or replacement
HIGHFDA DEVICE
Philips Recalls IntelliVue Patient Monitor Due to Alarm Failure
Philips North America recalled 1,913,441 IntelliVue Patient Monitors on October 31, 2025. The monitors may fail to alarm, posing serious risks to patients. Users must stop using the device immediately and follow the manufacturer's instructions.
Philips North America
Potential issue
HIGHFDA DEVICE
Philips IntelliVue MP90 Monitors Recalled Over Alarm Failure
Philips North America recalled 1,913,441 IntelliVue MP90 monitors on October 31, 2025. The monitors may fail to alarm, posing a high risk to patient safety. Users must stop using the devices immediately and follow manufacturer instructions for remedy.
Philips North America
Potential issue
HIGHFDA DEVICE
Philips Recalling IntelliVue Patient Monitors Over Alarm Failure
Philips North America recalled 1,913,441 IntelliVue Patient Monitors on October 31, 2025. A potential issue causes the monitors to fail to alarm, posing serious risks to patient safety. Consumers and healthcare providers should stop using these devices immediately and follow recall instructions.
Philips North America
Potential issue
HIGHFDA DRUG
Nivagen Zinc Oxide Ointment Recalled Over cGMP Deviations
Nivagen Pharmaceuticals recalled 7,920 bottles of Zinc Oxide Ointment on October 31, 2025. The recall follows cGMP deviations that could impact product safety. Consumers should cease use immediately and consult healthcare providers for advice.
NIVAGEN ZINC OXIDE
cGMP deviations
HIGHFDA FOOD
First & Last Tavern Puttanesca Sauce Recalled Over Botulism Risk
First & Last Tavern recalled 30 cases of Puttanesca Sauce on October 31, 2025. The product may be contaminated with Clostridium botulinum, a toxin that can cause severe illness. Consumers should stop using the sauce immediately and contact the company for a refund.
First & Last Tavern
May be
HIGHFDA DRUG
Trifecta Pharmaceuticals Recalls Clotrimazole Cream Over cGMP Issues
Trifecta Pharmaceuticals recalled 14,700 bottles of Globe Clotrimazole Cream USP on October 31, 2025, due to significant cGMP deviations. The affected product may not meet necessary safety and quality standards. Consumers should stop using the cream immediately and seek guidance from healthcare providers.
CLOTRIMAZOLE
cGMP deviations
HIGHFDA DRUG
Trifecta Pharmaceuticals Recalls Clotrimazole Cream for cGMP Violations
Trifecta Pharmaceuticals USA recalled 12,150 bottles of Globe Clotrimazole Cream on October 31, 2025. The recall stems from deviations in current Good Manufacturing Practices (cGMP). Consumers should stop using the cream immediately and contact their healthcare providers.
CLOTRIMAZOLE
cGMP deviations
HIGHFDA DRUG
Blossom Pharmaceuticals Recalls Lanashield Skin Barrier Over cGMP Violations
Blossom Pharmaceuticals recalled 9,600 containers of Lanashield Skin Barrier on October 31, 2025 due to cGMP deviations. Consumers and healthcare providers should stop using the product immediately. The recall affects products distributed nationwide in the USA.
Blossom Pharmaceuticals
cGMP deviations
HIGHFDA DRUG
Dynarex Recalls Moisturizing Wound Hydrogel Over cGMP Violations
Dynarex Corporation recalled 8,184 bottles of Dynagel Moisturizing Wound Hydrogel on October 31, 2025. The recall follows deviations from current Good Manufacturing Practices (cGMP). Consumers should stop using the product immediately and consult healthcare providers for guidance.
Blossom Pharmaceuticals
cGMP deviations
HIGHFDA FOOD
Indian Cookware Recalls Kadai Due to Lead Contamination Risk
Indian Cookware and Appliance LLC recalled 10 pieces of Aluminium Hammered Kadai on October 31, 2025. The products may contain leachable lead, posing a health risk. Consumers should stop using the product and seek a refund or replacement immediately.
INDIAN COOKWARE AND APPLIANCE
Potential contamination
HIGHFDA DRUG
Dynarex Recalls Zinc Oxide Ointment Over cGMP Deviations
Dynarex Corporation recalled 2,592 bottles of WeCare Zinc Oxide Ointment on October 31, 2025, due to cGMP deviations. The recall affects products distributed nationwide in the USA. Consumers and healthcare providers must stop using the ointment immediately and seek guidance.
ZINC OXIDE
cGMP deviations
HIGHFDA DRUG
Cipla Recalls Phytonadione Injectable Emulsion Due to Stability Issues
Cipla USA recalled 4,438 cartons of Phytonadione Injectable Emulsion on October 31, 2025. The product failed stability specifications, raising concerns about its safety. Consumers and healthcare providers must stop using the product immediately and seek guidance.
PHYTONADIONE
Failed Stability
HIGHFDA FOOD
Blonde Beard's Wing Sauce Recalled Due to Undeclared Soy
Blonde Beard's recalled 4,888 bottles of Dojo Asian Wing Sauce on October 31, 2025. The product contains undeclared soy, posing a risk to individuals with soy allergies. The sauce was distributed across multiple states and Canada.
Blonde Beard's
Undeclared Soy
HIGHFDA FOOD
First & Last Tavern Pasta Sauce Recalled Due to Botulism Risk
First & Last Tavern recalled 30 cases of meat-flavored pasta sauce on October 31, 2025. The product may be contaminated with Clostridium botulinum, a dangerous toxin. Consumers should not consume this product and should seek a refund or replacement.
First & Last Tavern
May be
HIGHFDA DEVICE
Philips Ultrasound System Recalled Over Compatibility Issues
Philips Ultrasound recalled 4,819 diagnostic ultrasound systems on October 31, 2025. The recall affects models 795005, 795161, and 989605449841 due to compatibility issues with Apple devices running iOS 18. These issues may prevent the systems from performing live imaging, posing risks in medical settings.
Philips Ultrasound
Ultrasound system
HIGHFDA DEVICE
Stryker Recalls Arise 1000EX Mattresses Over Compatibility Issues
Stryker recalled 289 Arise 1000EX mattresses on October 31, 2025. The recall affects products sold nationwide due to potential incompatibility with MV3 beds. Users should stop using these mattresses immediately.
Stryker Medical Division of Stryker
Stryker has
HIGHFDA DRUG
Dynashield Cream Recalled Due to cGMP Deviations
Dynashield, a 4 oz cream, is recalled after cGMP deviations were identified. The recall affects 7,944 units distributed nationwide. Consumers should stop using the product immediately and contact their healthcare provider for guidance.
DYNASHIELD
cGMP deviations
HIGHFDA DEVICE
Stryker Recalls NICO Myriad Handpieces Over Latex Allergy Risk
Stryker recalled 39,148 NICO Myriad Handpieces on October 31, 2025, due to a latex hazard. The packaging tape contains latex despite products being labeled latex-free. This poses a significant allergy risk to patients and healthcare providers.
Stryker
Tape used
HIGHFDA DEVICE
Philips Patient Monitor Recalled Over Alarm Malfunction
Philips North America recalled over 1.9 million IntelliVue Patient Monitors on October 31, 2025. The monitors may fail to sound alarms, posing a serious risk to patients. Healthcare providers must stop using these devices immediately and follow recall instructions.
Philips North America
Potential issue
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