1,817 pharmaceutical and medication recalls tracked. Stay informed about FDA drug safety alerts, prescription medications, over-the-counter drugs, and dietary supplements.
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Philips Medical Systems Nederland B.V. recalls 45 Allura Xper FD20/10 imaging systems worldwide due to internal component deterioration. The CMOS battery, hard disk drive and/or power supply may fail. Motorized movements can become unavailable while imaging remains possible. Stop using the device and follow manufacturer instructions.
Sun Pharmaceutical Industries recalled 1,870 kits nationwide after an out-of-specification dissolution test for sulphate in Sodium Tartrate Dihydrate used to produce Mertiatide. The recall affects Rx-only kits distributed across the U.S. Healthcare providers and patients should stop using the product immediately and follow guidance from Sun Pharmaceutical. Contact information is provided by the UQ
Chlorpromazine Hydrochloride Tablets, 200 mg, 100-count bottle, manufactured by Zydus Lifesciences Ltd. and distributed by Northstar Rx LLC, are under recall nationwide in the United States. The CGMP deviation involves elevated levels of N-Nitroso Desmethyl Chlorpromazine. Consumers should stop use and contact their healthcare provider.
Philips Medical Systems Nederland recalled 174 Allura Xper FD20 OR Tables worldwide, including 45 in the United States. The devices may deteriorate internally, rendering motorized movements inoperable. Hospitals and clinics should stop using the devices and follow the manufacturer's recall instructions.
The FDA confirms a nationwide recall of Zydus Lifesciences Chlorpromazine Hydrochloride tablets 200 mg (NDC 70710-1133-1) distributed by Zydus Pharmaceuticals USA. The recall cites CGMP deviations and the presence of N-Nitroso Desmethyl Chlorpromazine above acceptable intake. Consumers and healthcare providers should stop using the product immediately and contact the distributor for guidance.
Philips Medical Systems Nederland B.V. recalls 75 Allura Xper FD20/20 imaging systems due to potential deterioration of the CMOS battery, hard drive and power supply. Motorized movements could become unavailable while X-ray imaging remains functional. Operators should stop using affected units and follow manufacturer instructions.
Philips Medical Systems Netherlands B.V. recalled 3 Allura Xper FD20/20 OR Tables worldwide, including the US, on 2025-09-03 after detection of degradation in internal components. The recall cites CMOS battery, hard disk drive, and/or power supply unit deterioration. Motorized movements may fail while imaging remains available. The recall is active. Stop using the device following recall guidance.
Philips Medical Systems Nederland B.V. recalls 2 Allura Xper FD10 OR Tables worldwide. The devices may fail to perform motorized movements due to deterioration of internal components. Healthcare providers should stop using the devices and contact Philips for instructions.
Philips Medical Systems Nederland B.V. recalls 313 Allura Centron devices with model 722400 worldwide after a BIOS battery drains too quickly. The issue can halt the system start-up with no user warning. The recall was issued September 3, 2025 and remains active as of October 8, 2025. Consumers should contact Philips or their healthcare provider for instructions.
Philips Medical Systems Nederland B.V. recalls 8 medical tables worldwide due to BIOS battery depletion risk. The recall affects Allura Xper FD20/15 OR Tables with model number 722059. The BIOS battery may deplete faster than expected, causing the system not to start without warning. Hospitals and healthcare providers should stop using the device immediately and follow the recall instructions.
Philips Medical Systems Nederland B.V. recalls 5,067 Allura Xper FD20 imaging systems worldwide. The BIOS battery may deplete faster than planned, causing the system to fail to start. The issue affects 1,626 US and 3,441 international units. Customers should stop using affected devices and follow manufacturer instructions.
The FlexLab X System Potassium Test System was recalled by Inpeco S.A. on 2025-09-03 after the FDA identified an unvalidated hemolysis, icterus, and lipemia function in its Sample Integrity Module. The recall affects US distribution to California and New York. Stop using immediately and follow manufacturer instructions.
Viorele birth-control pills are recalled in the United States for failed impurity and degradation specifications. Glenmark Pharmaceuticals Inc. is distributing the issue nationwide, affecting 26,928 packs. Patients should stop using the product and contact a clinician for guidance.
Philips Medical Systems Nederland B.V. recalls Allura Xper FD20 Biplane OR Table models 722020 and 722025. Four units are affected worldwide, including two in the United States. The BIOS battery may deplete faster than expected, halting the system startup with no user warning. The recall advises stop-use and coordination with healthcare providers for instructions.
Philips Medical Systems Nederland recall 115 Allura Xper FD20/20 imaging systems worldwide after reports that the BIOS battery may deplete prematurely. The startup process may halt with no user alert. Hospitals and providers should stop using affected units and await manufacturer instructions.
Philips Medical Systems Nederland B.V. recalled 2 Allura Xper FD10C imaging systems in the United States. The BIOS battery may deplete faster during design, halting startup without warning. Hospitals should stop using the device and follow the manufacturer’s recall instructions.
Philips Medical Systems Nederland B.V. recalls 5 Allura Xper FD20/20 OR Tables (Model 722039) worldwide. The BIOS battery may deplete faster than designed, halting startup with no warning. Hospitals should stop using the affected devices and follow recall instructions from Philips.
Philips Medical Systems Nederland recalled 501 Allura Xper FD20 Biplane devices sold worldwide to hospitals and healthcare facilities. The BIOS battery may deplete faster during design, halting the startup and preventing the system from starting with no user messages. Healthcare providers and patients should stop using the device and follow the recall instructions from Philips.
Beckman Coulter recalled 2,146 units of the SYNCHRON Systems Phosphorus (PHOSm) Reagent due to calibration failures that may delay patient results. Specific reagent lots may not function properly before their expiration date. Healthcare providers and patients must stop using these reagents immediately and follow manufacturer instructions.
Inpeco recalled eight FlexLab FLX System Potassium Test System units sold in California and New York. The recall targets the Sample Integrity Module HIL function, which detects hemolysis, icterus and lipemia. The FDA has not evaluated this function for safety or effectiveness, risking erroneous results or delays. Labs should stop using the device immediately.
Philips Medical Systems Nederland B.V. recalls 2 Allura Xper FD10 OR Tables worldwide, including the United States. The BIOS battery may deplete faster than expected, halting the start-up with no user warning. Hospitals should stop using the devices and await recall instructions by letter.
Philips Medical Systems Nederland B.V. recalls 300 units of the Allura Xper FD20/15 with model 722058 after the BIOS battery may deplete prematurely, causing startup failure. The recall covers worldwide distribution. Patients and healthcare providers should stop using the device immediately and follow manufacturer instructions.
Philips Medical Systems Nederland B.V. recalled 585 units of the Allura Xper FD10/10 diagnostic system globally, including 145 in the United States, after reports that the BIOS battery can deplete faster than expected and halt system startup. The recall covers models 722005, 722011, and 722027. Healthcare facilities should stop using the device and follow manufacturer instructions for remediation.
Philips Medical Systems Nederland B.V. recalls 53 units of the Allura Xper CV20 system due to a BIOS battery that may deplete faster than designed. The recall affects units distributed worldwide, including the US and many other countries. The failure prevents system startup with no prior warning messages.
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