Drug Recalls Center

1,425 pharmaceutical and medication recalls tracked. Stay informed about FDA drug safety alerts, prescription medications, over-the-counter drugs, and dietary supplements.

1,425
Total Drug Recalls
24
High Risk Medications
FDA
Official Source

Important Medication Safety Information

  • Do not stop taking prescribed medications without consulting your healthcare provider
  • Contact your pharmacist or doctor if you have a recalled medication
  • Check lot numbers carefully - not all batches may be affected
  • Return recalled medications to your pharmacy for proper disposal

Looking for a specific drug? Use the search page to find recalls by medication name, manufacturer, or NDC number.

HIGHFDA DEVICE

SEDECAL Recalls Mobile X-ray System Over Cleaning Hazard

SEDECAL SA recalled eight mobile X-ray systems on June 10, 2025. The recall follows warnings that the devices are not water-resistant and must be cleaned per the manual. Users must stop using the device immediately to avoid potential injuries.

SEDECAL SA
Sedecal sent
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HIGHFDA DEVICE

SEDECAL SA Recalls Mobile X-ray System Over Water Resistance Hazard

SEDECAL SA recalled its Mobile X-ray system on June 10, 2025, due to a water resistance hazard. The company alerted users to strictly follow cleaning instructions to avoid potential harm. The recall affects devices distributed in California, Illinois, and New Jersey.

SEDECAL SA
Sedecal sent
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HIGHFDA DEVICE

SEDECAL SA Recalls Mobile X-ray System Over Cleaning Hazard

SEDECAL SA recalled 6 units of its Mobile X-ray system on June 10, 2025. The equipment is not water-resistant and improper cleaning may lead to serious risks. Patients and healthcare providers must stop using the device immediately and follow recall instructions.

SEDECAL SA
Sedecal sent
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HIGHFDA DEVICE

SEDECAL Recalls Mobile X-ray System Due to Cleaning Risks

SEDECAL SA recalled 1,198 units of its MobileDiagnost wDR 2.2 X-ray system on June 10, 2025. The equipment is not water-resistant and may pose hazards if not cleaned according to the manual. Users must stop using the device immediately and contact the manufacturer for further instructions.

SEDECAL SA
Sedecal sent
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HIGHFDA DEVICE

Sedecal Recalls Mobile X-ray System Due to Water Resistance Issues

Sedecal recalled nine units of its SM-40HF-Batt Mobile X-ray system on June 10, 2025, due to safety concerns. The equipment is not water-resistant and improper cleaning could lead to dangerous consequences. Patients and healthcare providers must stop using the device immediately.

SEDECAL SA
Sedecal sent
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HIGHFDA DEVICE

SEDECAL Recalls Mobile X-ray System Due to Water Resistance Issue

SEDECAL SA recalled 268 units of the Model Number 40KWFXPLUS Mobile X-ray system on June 10, 2025. The recall addresses concerns over improper cleaning and water resistance. Healthcare providers must stop using the device immediately and follow the manufacturer’s instructions.

SEDECAL SA
Sedecal sent
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HIGHFDA DEVICE

Sedecal Recalls Mobile X-ray System Over Water Resistance Issues

Sedecal recalled one mobile X-ray system on June 10, 2025, due to concerns about improper cleaning. The model SM-40HF-B-D-C is not water-resistant and poses risks if not cleaned according to instructions. Users must stop using the device immediately and follow recall instructions.

SEDECAL SA
Sedecal sent
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HIGHFDA DEVICE

SEDECAL SA Mobile X-ray System Recalled Over Cleaning Hazard

SEDECAL SA recalled 10 Mobile X-ray systems on June 10, 2025, due to a hazard related to improper cleaning. The equipment lacks water resistance, posing a risk to patients and healthcare providers. Users must stop using the device immediately and follow manufacturer instructions.

SEDECAL SA
Sedecal sent
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HIGHFDA DEVICE

SEDECAL Mobile X-ray System Recall Due to Hazardous Cleaning Risks

SEDECAL SA recalled one Mobile X-ray system on June 10, 2025, after warning that improper cleaning could lead to equipment failure. The device is not water-resistant and must be cleaned according to strict manual instructions. The recall affects units distributed in California, Illinois, and New Jersey.

SEDECAL SA
Sedecal sent
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HIGHFDA DEVICE

SEDECAL Recalls Mobile X-ray System Due to Water Resistance Issue

SEDECAL SA recalled 181 units of its Mobile X-ray system on June 10, 2025. The recall warns users that the equipment is not water-resistant and requires strict cleaning protocols. Improper cleaning may lead to serious consequences for patients and healthcare providers.

SEDECAL SA
Sedecal sent
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HIGHFDA DEVICE

SEDECAL Recalls Mobile X-ray System Over Cleaning Safety Hazard

SEDECAL SA recalled one unit of its mobile X-ray system on June 10, 2025. The system is not water-resistant and poses a high hazard risk due to improper cleaning. Users must stop using the device immediately and follow the recall instructions.

SEDECAL SA
Sedecal sent
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HIGHFDA DEVICE

SEDECAL SA Recalls Mobile X-ray System Due to Cleaning Hazard

SEDECAL SA recalled one Mobile X-ray system on June 10, 2025, due to improper cleaning instructions. The device is not water-resistant, posing a potential hazard for users. This recall serves as a reminder to follow all cleaning protocols strictly to avoid consequences.

SEDECAL SA
Sedecal sent
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HIGHFDA DEVICE

SEDECAL Recalls Mobile X-ray System Over Water Resistance Risks

SEDECAL SA recalled 12 units of its Mobile X-ray system on June 10, 2025, due to water resistance issues. Users must adhere to strict cleaning instructions to avoid equipment damage. The recall affects units distributed in California, Illinois, and New Jersey.

SEDECAL SA
Sedecal sent
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HIGHFDA DEVICE

SEDECAL Mobile X-ray System Recalled Due to Cleaning Hazard

SEDECAL SA recalled six units of its Mobile X-ray system on June 10, 2025. The device is not water-resistant and improper cleaning can lead to hazards. Healthcare providers must stop using the device immediately and follow recall instructions.

SEDECAL SA
Sedecal sent
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HIGHFDA DEVICE

SEDECAL Mobile X-ray System Recalled Over Water Resistance Issue

SEDECAL SA recalled eight units of its Mobile X-ray system on June 10, 2025. The recall follows warnings regarding improper cleaning due to the device's lack of water resistance. Users must stop using the equipment immediately to avoid potential hazards.

SEDECAL SA
Sedecal sent
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HIGHFDA DEVICE

SEDECAL Recalls Mobile X-ray System Over Cleaning Hazards

SEDECAL SA recalled 14 units of its SM-40HF-B-D-C mobile X-ray system on June 10, 2025. The company warned that the device is not water-resistant and improper cleaning can lead to serious consequences. Health care providers must stop using the equipment immediately and follow recall instructions.

SEDECAL SA
Sedecal sent
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HIGHFDA DEVICE

SEDECAL Recalls Mobile X-ray System Over Water Resistance Issue

Sedecal recalled 142 units of its SM-40HF-B-D-C Mobile X-ray system on June 10, 2025. The equipment is not water-resistant and requires strict cleaning protocols to prevent hazards. Improper cleaning can lead to potentially dangerous consequences for patients and healthcare providers.

SEDECAL SA
Sedecal sent
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HIGHFDA DEVICE

Sedecal Recalls Mobile X-ray System Over Cleaning Hazard

Sedecal recalled two units of its Mobile X-ray system on June 10, 2025. Users must stop using the device due to improper cleaning risks. The equipment is not water-resistant, posing a high hazard to patients and healthcare providers.

SEDECAL SA
Sedecal sent
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