immediate action Recalls

GET TESTED INTERNATIONAL AB Recalls Food Intolerance Test Due to Approval Issues

Distribution without premarket approval/clearance.

GET TESTED INTERNATIONAL AB Recalls Allergy Test Over Approval Issues

GET TESTED INTERNATIONAL AB recalled 76 units of its Allergy Test on November 3, 2025. The recall occurred due to distribution without premarket approval. Patients and healthcare providers should stop using the device immediately.

GET TESTED INTERNATIONAL AB Recalls Candida Test for Lack of Approval

GET TESTED INTERNATIONAL AB recalled 109 units of its Candida Test on November 3, 2025. The recall stems from distribution without premarket approval or clearance. Patients and healthcare providers should stop using this device immediately.

GET TESTED INTERNATIONAL AB Serotonin Test Recall 12 Units (2025)

Distribution without premarket approval/clearance.

GET TESTED INTERNATIONAL AB Syphilis Test Recalled in 2025 for PMA Lapse Nationwide

Distribution without premarket approval/clearance.

GET TESTED INTERNATIONAL AB Drug Test Small (4 Substances) Recall 2025

GET TESTED INTERNATIONAL AB distributed 1 unit nationwide in the United States. The device lacked premarket approval or clearance. Stop using the product immediately and contact GET TESTED INTERNATIONAL AB for instructions.

GET TESTED INTERNATIONAL AB Kidney Test Recalled for 100 Units in 2025

Distribution without premarket approval/clearance.

GET TESTED INTERNATIONAL AB DHEA Test Recalled for Premarket-Approval Lapse, 17 Units (2025)

Distribution without premarket approval/clearance.

Medtronic MiniMed 780G Insulin Pump Recalled Over Software Issue

A software timing and processor communication issue in MiniMed" 780G software version 6.60 may trigger Pump Error 43 and/or Pump Error 41, resulting in suspension of insulin delivery.

Stryker MV3 Bariatric Bed Recalled Over Compatibility Issues

Stryker Medical recalled 286 MV3 bariatric beds on October 31, 2025. The beds may not be compatible with Arise 1000EX mattresses, posing risks to patients. Healthcare providers and patients must stop using the beds immediately.

Nivagen Zinc Oxide Ointment Recall 912 Containers Over cGMP Deviations (2025)

First & Last Tavern Puttanesca Sauce Recalled Over Botulism Risk

May be contaminated with Clostridium botulinum

First & Last Tavern Marinara Sauce Recalled Over Botulism Risk

First & Last Tavern recalled 30 cases of marinara sauce on October 31, 2025. The sauce may be contaminated with Clostridium botulinum, posing a high health risk. Consumers should not consume the product and seek refunds or replacements.

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.

Philips IntelliVue MX700 Recall Affects 1,913,441 Monitors Worldwide (2025)

Potential issue where the IntelliVue monitors did not alarm.

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.

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.

Philips IntelliVue MX100 Patient Monitors Recalled for Alarm Failure (Z-0861-2026)

Potential issue where the IntelliVue monitors did not alarm.

PHILIPS IntelliVue MP80 Recall 1,913,441 Monitors Worldwide for Alarm Failure (2025)

Potential issue where the IntelliVue monitors did not alarm.

Nivagen Zinc Oxide Ointment Recalled Due to cGMP Deviations