electrical hazard Recalls

1,120 recalls tagged with “electrical hazard”.

Health & Personal Care
HIGH
FDA DEVICE

I.T.S. GmbH Recalls 15,517 FLS Foot Locking Plates System and Hallux Osteotomy Plates Over MRI Heat‑

I.T.S. GmbH recalled 15,517 FLS Foot Locking Plates System and HOL Hallux Osteotomy locking plates distributed nationwide in the United States. Updated MRI safety testing shows higher RF-induced temperature increases under certain MRI conditions than previously reflected in the IFU. Patients and healthcare providers should stop using this device immediately and follow the recall instructions from:

I.T.S. GmbH
Updated MRI
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Health & Personal Care
HIGH
FDA DEVICE

ITS Recalls 70 Olecranon Plates Over MRI RF Heating Risk (2026)

ITS recalls 70 Olecranon Plates with Angular Stability distributed nationwide in the United States. Updated MRI safety testing shows higher RF-induced temperature increases under certain MRI conditions than described in the IFU. Patients and healthcare providers should stop using this device immediately and contact ITS or their healthcare provider for instructions.

I.T.S. GmbH
Updated MRI
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Health & Personal Care
HIGH
FDA DEVICE

ITS GmbH Recalls 623 HCS Headless Cannulated Screws Over MRI Heating Risk (2026)

ITS GmbH recalled 623 HCS Headless Cannulated Screws distributed nationwide to U.S. healthcare facilities. The defect involves higher RF-induced temperature increases during certain MRI procedures than the IFU described. Affected patients and providers should stop using immediately and follow recall instructions. Contact ITS GmbH or your healthcare provider for instructions.

I.T.S. GmbH
Updated MRI
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Health & Personal Care
HIGH
FDA DEVICE

ITS GmbH HLS Hand Locking Plates System Recalled for MRI Heating Risk (1,307 Units, 2026)

ITS GmbH recalled 1,307 units of the HLS Hand Locking Plates System distributed nationwide in the United States after MRI safety testing showed higher RF-induced temperature increases. The issue exceeds what is described in the IFU under certain MRI conditions. Patients and healthcare providers should stop using the device immediately and follow ITS GmbH's recall instructions.

I.T.S. GmbH
Updated MRI
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Recalled Matrix Retail T30 (TM729) Treadmill
HIGH
CPSC

Johnson Health Tech Expands Treadmill Recall Over Fire Hazard

Johnson Health Tech expanded its recall of Matrix and Vision treadmills due to fire hazards. The affected models include T30, TF30, T50, TF50, T75, and others. Consumers should stop using these treadmills immediately and check for a power cord bracket.

Johnson Health Tech Expands
The power
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Health & Personal Care
HIGH
FDA DEVICE

Stryker Recalls MOLLI 2 Surgical Markers Over Dislodging Risk

Stryker recalled 5,864 units of the MOLLI 2 surgical markers on January 21, 2026. The recall follows concerns that magnetic surgical tools may dislodge markers during procedures. Healthcare providers and patients must stop using these devices immediately.

Stryker
Due to
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Health & Personal Care
HIGH
FDA DEVICE

Auris Health Recalls Bronchoscopy Device Over Software Issue

Auris Health recalled 173 bronchoscopy devices due to a software malfunction. This issue could lead to improper robotic arm positioning, risking patient safety. The recall affects devices distributed nationwide and in Canada, with the announcement made on January 21, 2026.

Auris Health
Device for
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Health & Personal Care
HIGH
FDA DEVICE

Agiliti Recalls Adapt Pump Over Microclimate Management Failure

Agiliti Health recalled 4,286 Adapt Pumps on January 21, 2026, after identifying a malfunction. The issue prevents the Microclimate Management function from re-engaging following the Autofirm function. This defect poses a risk to patients relying on the device for safe pressure management.

Agiliti Health - Ellis
Agiliti identified
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Health & Personal Care
HIGH
FDA DRUG

Dukal BZK Antiseptic Towelettes Recalled for CGMP Deviations (2026)

Nationwide recall of Dukal BZK Antiseptic Towelettes due to CGMP deviations. The products are manufactured for Dukal, LLC in Ronkonkoma, NY and distributed across the United States. Stop using immediately and contact ACME United Corporation for guidance.

Dukal
CGMP Deviations
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Health & Personal Care
HIGH
FDA DEVICE

Instrumentation Laboratory GEM Premier 5000 GEM PAK Recall Affects 74 Units Worldwide

A worldwide distribution recall covers 74 GEM PAK cartridges for the GEM Premier 5000. The issue involves PCSND errors during warm-up that can trigger ejection of GEM PAKs and may delay results. Institutions should follow recall instructions from Instrumentation Laboratory and notify healthcare teams immediately.

Instrumentation Laboratory
Confirmed customer
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Health & Personal Care
HIGH
FDA DEVICE

Instrumentation Laboratory GEM Premier 5000 PAK Recall 2026 for 51 Units

Instrumentation Laboratory recalled 51 GEM Premier 5000 PAK cartridges worldwide after complaints of PCSND errors during warm-up. These errors can cause GEM PAK cartridges to eject. The recall could delay results and affect patient management. Stop using the affected cartridges and follow recall instructions from Instrumentation Laboratory.

Instrumentation Laboratory
Confirmed customer
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Health & Personal Care
HIGH
FDA DEVICE

Instrumentation Laboratory Recalls GEM Premier 5000 GEM PAK Cartridges Over PCSND Errors, 1,989 US/3

GEM Premier 5000 recall announced for 1,989 units distributed worldwide, including the US and numerous other countries. The issue involves GEM PAK cartridges experiencing Process Control Solution Not Detected errors during warm-up, causing ejections and potential delays in patient results. Stop using the device and follow manufacturer recall instructions.

Instrumentation Laboratory
Confirmed customer
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Health & Personal Care
HIGH
FDA DEVICE

Instrumentation Laboratory Recalling 10 GEM Premier 5000 PAK Cartridges for PCSND Error During Warm‑

Instrumentation Laboratory recalled 10 GEM Premier 5000 PAK cartridges sold worldwide after reports of increased PCSND errors during warm‑up. The issue can cause GEM PAK ejections and delays in results. Clinicians and labs should follow the manufacturer’s recall instructions and seek guidance from their healthcare provider.

Instrumentation Laboratory
Confirmed customer
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Health & Personal Care
HIGH
FDA DEVICE

Instrumentation Laboratory Recalling 1,126 GEM PAK Cartridges for GEM Premier 5000 Over PCSND Errors

Instrumentation Laboratory issued a high-severity recall for 1,126 GEM PAK cartridges used with the GEM Premier 5000. The recall cites increased PCSND errors during warm-up that can cause consecutive GEM PAK ejections. The issue may delay patient results. Hospitals should halt use and follow manufacturer instructions immediately.

Instrumentation Laboratory
Confirmed customer
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Health & Personal Care
HIGH
FDA DEVICE

Instrumentation Laboratory Recalls 352 GEM PAK Cartridges for GEM Premier 5000 Over PCSND Errors

Instrumentation Laboratory recalls 352 GEM PAK cartridges for the GEM Premier 5000 worldwide due to increased PCSND errors during warm-up, risking delayed results. Medical facilities should stop using affected GEM PAKs and follow recall instructions. Manufacturers will provide further guidance to healthcare providers and patients.

Instrumentation Laboratory
Confirmed customer
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Tag Statistics

Total Recalls
1,120

Related Tags

burn riskimmediate actionstop use immediatelyrepair availablereplacement availablefda regulatedcpsc regulatedreturn for refundfederal law violationsuffocation riskinfant productadult product