immediate action Recalls

2,679 recalls tagged with “immediate action”.

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
Read more
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
Sedecal sent
Read more
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
Sedecal sent
Read more
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
Sedecal sent
Read more
Health & Personal Care
HIGH
FDA DEVICE

SEDECAL SA Recalled Mobile X-ray System Over Cleaning Hazard (2025)

Sedecal recalled 1 Mobile X-ray system due to major safety concerns. The device is not water-resistant and improper cleaning can cause malfunctions. Healthcare providers and patients must stop using the system immediately and follow manufacturer instructions.

SEDECAL SA
Sedecal sent
Read more
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
Sedecal sent
Read more
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
Sedecal sent
Read more
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.

Sedecal
Sedecal sent
Read more
Health & Personal Care
HIGH
FDA DEVICE

Sedecal SM-40HF-B-D-C 40KW Mobile X-ray System Recalled for Cleaning Water-Resistance Issue (2025)

Sedecal SA recalled 39 mobile X-ray systems due to a cleaning instruction issue that could cause improper maintenance. The recall affects units in the US and Canada. An email to consignees emphasizes the device is not water-resistant and must be cleaned per the manual, outlining potential consequences of improper cleaning. Healthcare facilities should stop using the device immediately and followSE

Sedecal SA
Sedecal sent
Read more
Health & Personal Care
HIGH
FDA DEVICE

Sedecal SM-40HF-B-D-C 40KW Mobile X-ray System Recall 2025

Sedecal SA recalled 4 units of the SM-40HF-B-D-C 40KW Mobile X-ray System distributed to U.S. facilities in California, Illinois and New Jersey. The equipment is not water-resistant and must be cleaned strictly according to the manual. Facilities should stop using the device immediately and follow the manufacturer’s recall instructions.

Sedecal SA
Sedecal sent
Read more
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
Sedecal sent
Read more
Health & Personal Care
HIGH
FDA DEVICE

Sedecal Mobile X-ray System Recall for 1 Unit Over Water Exposure Cleaning Hazard (2025)

Sedecal SA recalls 1 unit of Model 40KWMOBILE3.899 Mobile X-ray system distributed to consignees in the United States, including California, Illinois and New Jersey. The device is not water-resistant and must be cleaned strictly according to the manual, with the notice outlining the potential consequences of improper cleaning. Healthcare providers and patients should stop using the device immediat

Sedecal
Sedecal sent
Read more
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
Sedecal sent
Read more
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
Sedecal sent
Read more
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
Sedecal sent
Read more
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
Sedecal sent
Read more
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
Sedecal sent
Read more
Health & Personal Care
HIGH
FDA DEVICE

Sedecal 40KWFX Mobile X-ray System Recall Affects 55 US Units (2025)

Sedecal recalled 55 Mobile X-ray System units sold to facilities in California, Illinois and New Jersey. The devices are not water-resistant and must be cleaned exactly as described in the manual, with clear warnings about the consequences of improper cleaning. Hospitals and healthcare providers should stop using the device immediately and follow Sedecal's recall instructions.

Sedecal
Sedecal sent
Read more
    immediate action Recalls | RecallRadar