All Product Recalls

Browse through 2,959 product recalls and safety alerts. Filter by hazard level, status, or search for specific products.

Health & Personal Care
HIGH
FDA DEVICE

Sedecal SA Recalls 181 SM-40HF-B-D-C Mobile X-ray Systems for Cleaning Not Water-Resistant Risk (202

Sedecal SA recalls 181 SM-40HF-B-D-C mobile X-ray systems in 2025 after concerns about cleaning and water resistance. The device is not water-resistant and must be cleaned strictly according to the manual. Manufacturers warn of potential consequences if cleaning is not followed. Hospitals and clinics should stop using the device and follow recall instructions immediately.

Sedecal
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Health & Personal Care
HIGH
FDA DEVICE

Sedecal Mobile X-ray System Recall for Not Water-Resistant Design Affects 10 Units (2025)

Sedecal SA recalls 10 SM-40HF-B-D-C mobile X-ray systems distributed in California, Illinois and New Jersey. The recall stems from a warning that the equipment is not water-resistant and must be cleaned strictly according to the manual. Hospitals and providers should stop using the device immediately and contact Sedecal for instructions.

Sedecal
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Health & Personal Care
HIGH
FDA DEVICE

Sedecal SA Recalls 17 SM_40HF_B_D_VIR3 Mobile X-ray Systems Over Water-Resistance Cleaning Risk (202

Sedecal SA recalled 17 SM_40HF_B_D_VIR3 Mobile X-ray systems distributed in California, Illinois and New Jersey after emailing consignees that the equipment is not water-resistant and must be cleaned exactly as the manual directs. The notices warn about consequences of improper cleaning. Hospitals and clinics should stop using the device and follow the recall instructions from Sedecal SA or their

Sedecal SA
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Health & Personal Care
HIGH
FDA DEVICE

Sedecal SA SM-40HF-B-D-C Mobile X-ray System Recalled for Cleaning Not-Water-Resistant Risk (142 US)

Sedecal SA recalled 142 SM-40HF-B-D-C 40KW mobile X-ray systems sold to consignees in California, Illinois and New Jersey. Sedecal warned the units are not water-resistant and must be cleaned exactly as the manual prescribes, outlining the consequences of improper cleaning. Hospitals and clinics should stop using the devices immediately and follow the manufacturer's recall instructions.

Sedecal
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Health & Personal Care
HIGH
FDA DEVICE

Sedecal SM-32HF-B-D-C 32KW Mobile X-ray System Recall Expanded (2025)

Sedecal SA recalled 8 SM-32HF-B-D-C 32KW 50G Mobile X-ray systems sold in the US and Canada after notifying consignees by email that the equipment is not water-resistant and must be cleaned strictly per the manual. The notice outlines possible consequences of improper cleaning. Hospitals should stop using the devices immediately and follow the recall instructions.

SEDECAL SA
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Health & Personal Care
HIGH
FDA DEVICE

Sedecal SM-40HF-B-D-C Mobile X-ray System Recall for Cleaning Risk (2025)

Sedecal recalled 2 units of the SM-40HF-B-D-C 40KW 55G/60G Mobile X-ray system after warning consignees that the device is not water-resistant and must be cleaned exactly according to the manual. The notice outlines the potential consequences of improper cleaning. Healthcare facilities in California, Illinois and New Jersey should stop using the device immediately and contact Sedecal for further 1

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Health & Personal Care
HIGH
FDA DEVICE

Sedecal Mobile X-ray Systems Recall 6 Units for Cleaning Not Water-Resistant Risk (2025)

Sedecal SA recalled 6 mobile X-ray systems in the United States on June 10, 2025 after warning that the devices are not water-resistant and must be cleaned strictly per the manual. The recall notes possible consequences of improper cleaning. Healthcare facilities should stop using the devices immediately and follow Sedecal's recall instructions.

Sedecal
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Health & Personal Care
HIGH
FDA DEVICE

Sedecal Recalled 7 Mobile X-ray Systems Over Cleaning Not Water-Resistant Issue (2025)

Sedecal recalled 7 mobile X-ray systems distributed to California, Illinois and New Jersey after warning that the equipment is not water-resistant and must be cleaned strictly per the manual. The notice highlights potential consequences of improper cleaning. Hospitals and clinicians should stop using the device and follow the manufacturer’s recall instructions.

Sedecal SA
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Health & Personal Care
HIGH
FDA DEVICE

Sedecal MobileDiagnost wDR 2.2 Recall for 1,198 Units in 2025

Sedecal recalled 1,198 MobileDiagnost wDR 2.2 mobile X-ray systems distributed in California, Illinois and New Jersey. The company reminded users the equipment is not water-resistant and must be cleaned strictly according to the manual. Improper cleaning could have consequences outlined by Sedecal. Health care providers should stop using the device immediately and follow recall instructions.

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Health & Personal Care
HIGH
FDA DEVICE

Sedecal RADPRO MOBILE Mobile X-ray System Recall Affects 24 Units in 2025

Sedecal SA recalls 24 RADPRO MOBILE mobile X-ray systems distributed in California, Illinois and New Jersey. A vendor notice warns the equipment is not water-resistant and must be cleaned strictly per the manual. Improper cleaning could have harmful consequences. Hospitals and clinics should stop using the device immediately and follow the manufacturer’s recall instructions.

Sedecal SA
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Health & Personal Care
HIGH
FDA DEVICE

SEDECAL SA SM_40HF_BDC Mobile X-ray System Recall Expanded in 2025 (1 Unit)

Sedecal SA recalled 1 unit of the SM_40HF_BDC Mobile X-ray System distributed in California, Illinois and New Jersey after notifying consignees that the unit is not water-resistant and must be cleaned strictly per the manual. The notice cites potential consequences of improper cleaning. Hospitals and providers should stop using the device and follow the manufacturer’s recall instructions.

SEDECAL SA
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Health & Personal Care
HIGH
FDA DEVICE

Sedecal SA Recalled 6 Mobile X-ray Systems for Water-Resistance Cleaning Issue (2025)

Sedecal SA recalled 6 SM-40HF-B-D-C mobile X-ray systems distributed to consignees in California, Illinois and New Jersey after a notice reminded users the devices are not water-resistant and must be cleaned strictly per the manual. The reminder outlined possible consequences of improper cleaning. Hospitals should stop using the devices and follow the manufacturer’s recall instructions.

Sedecal SA
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Health & Personal Care
HIGH
FDA DEVICE

SEDECAL SA Mobile X-ray System SM_40HF_BDC3 Recalled for Cleaning Risk (1 Unit, 2025)

SEDECAL SA recalled 1 unit of SM_40HF_BDC3 Mobile X-ray System distributed in California, Illinois and New Jersey. The device is not water-resistant and must be cleaned strictly per the manual. Healthcare facilities should stop using the device immediately and follow the manufacturer’s recall instructions.

SEDECAL SA
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Health & Personal Care
LOW
FDA DEVICE

Sedecal SA Recalls 12 40KWFXPLUS-710CW Mobile X-ray Systems for Cleaning Risk (2025 Recall)

Sedecal SA recalled 12 units of the 40KWFXPLUS-710CW Mobile X-ray system distributed to CA, IL and NJ. The recall cites that the equipment is not water-resistant and must be cleaned strictly per the manual to avoid consequences of improper cleaning. Hospitals and clinics should stop using the device immediately and follow the manufacturer’s recall instructions.

Sedecal SA
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Health & Personal Care
HIGH
FDA DEVICE

Sedecal SA Recalls 9 SM-40HF-Batt Mobile X-ray Systems (2025)

Sedecal SA is recalling 9 units of the SM-40HF-Batt 40KW analog Mobile X-ray System distributed in California, Illinois and New Jersey. The company sent an email to consignees warning the equipment is not water-resistant and must be cleaned strictly per the manual. Improper cleaning could cause system damage. Hospitals and clinics should stop using the devices immediately and contact Sedecal SA or

Sedecal SA
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Health & Personal Care
HIGH
FDA DEVICE

Sedecal Mobile X-ray System Recall: 3 Units Not Water-Resistant (2025)

Sedecal SA recalled 3 units of the SM_40HF_B_D_VIR3.004 Mobile X-ray system distributed to consignees in California, Illinois and New Jersey. The devices are not water-resistant and must be cleaned strictly per the manual. Patients and healthcare providers should stop using the device immediately and follow recall instructions.

Sedecal
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Health & Personal Care
HIGH
FDA DEVICE

SEDECAL SA Recalls 1 Unit SM-40HF-B-D-C Mobile X-ray System (2025)

SEDECAL SA recalled 1 unit SM-40HF-B-D-C 40KW 70C EN Mobile X-ray System after emailing consignees that the equipment is not water-resistant and must be cleaned per the manual. The notice outlines possible consequences of improper cleaning. Hospitals and providers should stop using the device immediately and follow the manufacturer’s recall instructions.

SEDECAL
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Health & Personal Care
HIGH
FDA DEVICE

Sedecal SA 40KWFXPLUS.002 Mobile X-ray System Recalled in 2025 (8 Units)

Sedecal SA recalled 8 mobile X-ray units in the United States after notifying consignees that the equipment is not water-resistant and must be cleaned strictly per the manual. The notice warns that improper cleaning could have consequences described in the manual. Healthcare providers and patients should stop using the devices immediately and contact Sedecal SA or their healthcare provider for the

Sedecal
Sedecal sent
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Health & Personal Care
HIGH
FDA DEVICE

Sedecal SA Recalls 22 SM-32HF-Batt Mobile X-ray Systems for Cleaning Risk (2025)

Sedecal SA recalled 22 SM-32HF-Batt 32KW analog mobile X-ray systems distributed to California, Illinois and New Jersey. The units are not water-resistant and must be cleaned strictly per the manual, with explicit consequences for improper cleaning. Healthcare facilities should stop using the devices immediately and follow the manufacturer's recall instructions sent by email.

Sedecal SA
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