fall hazard Recalls

102 recalls tagged with “fall hazard”.

Health & Personal Care
HIGH
FDA DEVICE

GE Healthcare Elscint Helix Dual-Head Gamma Camera Recall for Detector Fall Risk (3 Units Worldwide,

GE HealthCare Israel, Functional Imaging recalled 3 Elscint Helix dual-head gamma cameras worldwide. If moved without adequate detector support, mounting stress could cause a detector fall and life-threatening injury. Hospitals should stop using the device immediately and contact GE Medical Systems Israel, Functional Imaging for instructions.

GE Healthcare Israel Functional Imaging
GE HealthCare
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Health & Personal Care
HIGH
FDA DEVICE

GE HealthCare Recalls 102 Dual-Head Gamma Cameras for Cardiac Imaging (2025)

GE HealthCare recalled 102 dual-head gamma cameras used for cardiac imaging worldwide after finding that some systems past the End of Guaranteed Service could be moved without adequate detector support. This could place excessive stress on detector mounting mechanisms and may cause a detector to fall, posing life-threatening risk. Hospitals and healthcare providers should stop using the devices IM

GE HealthCare
GE HealthCare
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Recalled URMYWO Baby Lounger – Grey Feather
HIGH
CPSC

URMYWO Baby Loungers Recalled for Suffocation and Fall Hazards; 2025 Recall Active

URMYWO recalled its baby loungers on 2025-09-04 after reports of suffocation and fall hazards. The recall targets URMYWO loungers style grey feather sold via Amazon by Pomona. The devices fail to meet infant sleep standards due to short side walls and excessive pad thickness. Consumers should stop using the loungers and request a full refund.

URMYWO
The baby
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Recalled Nimbus Lock Carabiners
HIGH
CPSC

C.A.M.P. Nimbus Lock Carabiners Recalled for Fall Hazard in 2025

Camp USA recalled Nimbus Lock Carabiners sold through various retailers after a safety concern over the automatic closing mechanism. The carabiner's automatic closing mechanism can break and prevent the gate from closing, creating a fall risk. Stop using the recalled carabiners immediately and contact CAMP for inspection, repair or replacement.

Nimbus
The carabiner's
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Health & Personal Care
HIGH
FDA DEVICE

Boston Scientific Pacemakers Recall 28,911 U128 ACCOLADE, VISIONIST VALITUDE CRT-P Devices (2025)

Boston Scientific recalled 28,911 pacemakers worldwide due to a software flaw in Safety Architecture that could prevent Safety Mode when battery impedance is high. The recall covers ACCOLADE family devices and VISIONIST and VALITUDE CRT-Ps. Patients should stop using the device immediately and follow the recall letter instructions.

Boston Scientific
Software to
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Health & Personal Care
HIGH
FDA DEVICE

Philips CT Systems Recalled for Descent Hazard In 210-Unit Worldwide Distribution (2025)

Philips North America recalls 210 CT systems worldwide after reports that the patient support couch may descend unexpectedly to the lowest position following a replacement. Philips issued a recall dated 2025-08-13 with active status. The recall number is Z-2598-2025. Stop using immediately and follow manufacturer instructions.

Philips North America
The patient
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Health & Personal Care
HIGH
FDA DEVICE

Philips Ingenuity CT Brazil 728325 CT System Recalled for 3 Units in 2025

Philips recalled 3 Ingenuity CT Family Brazil systems, Model 728325, distributed worldwide, including the United States. A ball screw misalignment after a replacement may cause the patient support table to descend to the lowest position. Hospitals and clinicians should stop using the device and follow Philips recall instructions.

Philips
The patient
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Health & Personal Care
HIGH
FDA DEVICE

Philips Brilliance iCT SP CT Systems Recalled for Descending Couch Hazard in 14 Units Worldwide (202

Philips recalled 14 Brilliance iCT SP CT systems, model 728311, sold worldwide including the United States. The patient support couch may descend unexpectedly to the lowermost position because of ball screw misalignment after a replacement. Hospitals should stop using the device immediately and await manufacturer instructions.

Philips
The patient
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Health & Personal Care
HIGH
FDA DEVICE

Philips IQon Spectral CT 728332 Recalled Globally for Descending Patient Table Hazard

Philips North America has issued a recall for 81 IQon Spectral CT systems, Model 728332, sold worldwide. The patient support table may descend unexpectedly to the lowest position due to ball screw misalignment after a replacement. Stop using the device immediately and follow manufacturer recall instructions.

Philips North America
The patient
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Health & Personal Care
HIGH
FDA DEVICE

Philips Brilliance CT Systems Recalled for Descent Hazard in 2025 (73 Units)

Philips recalled 73 Brilliance CT systems worldwide after determining a ball screw misalignment could cause the patient couch to descend to the lowermost position. The recall covers Brilliance 16 Power, 728240; Brilliance CT 16 Slice, 728246; and Brilliance CT 6 Slice, 728256. Hospitals and clinics should stop using the devices and follow the manufacturer’s recall instructions immediately.

Philips
The patient
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Health & Personal Care
HIGH
FDA DEVICE

Philips CT Systems Brilliance 40/64 Channel and Ingenuity Flex Recalled for Couch Descent Risk (2025

Philips North America LLC is recalling 181 CT systems worldwide, including Brilliance CT 40 Channel 728235, Brilliance CT 64 Channel 728231, and Ingenuity Flex 728317. The patient support couch may descend to the lowermost position after a replacement. Hospitals and imaging centers should stop using the devices immediately and await recall instructions.

Philips
The patient
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Health & Personal Care
HIGH
FDA DEVICE

Philips Ingenuity CT System Recall 2025: 285 Units Worldwide

Philips recalled 285 Ingenuity CT systems worldwide, including 728321, 728323 and 728326 models. A ball screw misalignment after a replacement can cause the patient couch to descend to the lowermost position. Hospitals and clinics should stop using the devices and follow Philips recall instructions.

Philips
The patient
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Health & Personal Care
HIGH
FDA DRUG

Hospira Epinephrine Injection Vials Recalled for Lack of Sterility Assurance (2025)

Hospira recalls 49,620 vials of Epinephrine Injection, distributed nationwide in the United States. The recall, active since August 4, 2025, targets vials with NDC 0409-4933-05 and case NDC 0409-4933-10. The hazard is lack of assurance of sterility. Health professionals should stop using the product and contact Pfizer or a healthcare provider for guidance.

Epinephrine
Lack of
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Recalled Cosco 2-Step Kitchen Stepper model 11349WHG1E
MEDIUM
CPSC

Cosco 2-Step Kitchen Stepper Recall 2025 — 10 Models Affected

Dorel Home Furnishings recalls Cosco 2-Step Kitchen Steppers sold at multiple retailers after reports that the safety bar can detach or break during use. The recall covers 10 model numbers. Consumers should stop using the safety bar immediately and contact Dorel for a free repair kit.

Dorel Home Furnishings
The safety
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Tag Statistics

Total Recalls
102

Related Tags

immediate actionreturn for refundelectrical hazardstop use immediatelyreplacement availablecpsc regulatedfda regulatedinfant productsuffocation riskburn riskpoisoning riskpet related