workplace Recalls

35 recalls tagged with “workplace”.

Recalled Shenzhen Shijingjie Network Technology Extension Cord – blue
HIGH
CPSC

Shenzhen Shijingjie Network Technology Male-to-Male Extension Cords Recalled in 2026 Walmart Recall

Shenzhen Shijingjie Network Technology recalled two models of male-to-male extension cords sold at Walmart after safety concerns. The cords pose a risk of electrocution and carbon monoxide poisoning when used for backfeeding from a generator into a home. Consumers should stop using the recalled cords immediately and contact the company for a full refund.

Shenzhen Shijingjie Network Technology Male-to-Male Extension Cords
The recalled
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Recalled Noah Office Chair (Model number: M70160)
MEDIUM
CPSC

Tainoki Fine Furniture Recalls 3 Office Chairs Over Fall Hazard (2026)

Tainoki Fine Furniture recalled three office chairs sold at HomeGoods stores nationwide from August 2025 through December 2025 for about $180 to $200. The base can bend, creating a fall hazard. Stop using the chairs immediately and follow the recall instructions on the company site for a full refund.

Tainoki Fine Furniture
The recalled
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Health & Personal Care
HIGH
FDA DEVICE

Straumann USA Recalls 13 Custom Abutment Ti RC for TAN Material Mix-Up (2026)

Straumann USA recalled 13 Custom Abutment Ti RC units distributed worldwide, including the United States and Canada. A TAN material was misidentified as Titanium Ti Gr4 D during manufacturing, causing RC Titanium abutments to be made from TAN material. Clinics and patients should stop using the devices immediately and follow recall instructions from Straumann USA or their healthcare providers.

Straumann USA
A material
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Health & Personal Care
HIGH
FDA DEVICE

Philips Medical Systems Nederland recall 296 Allura Xper FD20/15 Imaging Systems Over Foot Switch Fl

Philips Medical Systems Nederland B.V. recalls 296 Allura Xper FD20/15 imaging systems distributed nationwide and internationally after reports the wired foot switch may fail to initiate imaging or start intermittently. The defect can delay X-ray imaging in patient care. Healthcare providers and patients should stop using the device and follow recall instructions from the manufacturer.

Philips Medical Systems Nederland B.V.
Philips has
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Health & Personal Care
HIGH
FDA DEVICE

Philips ALLURA Xper FD20 Recall for 5,084 Units Over Intermittent X-ray Imaging (2026)

Philips Medical Systems Nederland B.V. recalled 5,084 ALLURA Xper FD20 imaging systems sold nationwide and internationally after finding that the wired foot switch may fail to initiate X-ray imaging or perform intermittently. The defect can delay or interrupt imaging during patient care. Healthcare facilities should stop using the devices and follow the manufacturer’s recall instructions.

Philips Medical Systems Nederland B.V.
Philips has
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Health & Personal Care
HIGH
FDA DEVICE

Philips ALLURA Xper FD20 OR Table Recalled Worldwide; 196 Units Affected (2026)

Philips Medical Systems Nederland B.V. recalled 196 ALLURA Xper FD20 OR Tables sold to hospitals nationwide and internationally. The defect may prevent X-ray imaging from starting or cause intermittent operation when using the wired foot switch. Hospitals should stop using the devices and follow the recall instructions sent by letter.

Philips Medical Systems Nederland B.V.
Philips has
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Health & Personal Care
HIGH
FDA DEVICE

Philips Allura Xper FD20/20 Recall 111 Systems Worldwide Over Intermittent Imaging (2026)

Philips Medical Systems Nederland B.V. recalls 111 Allura Xper FD20/20 imaging systems with System Code 722038. The recall covers 31 units in the United States and 80 abroad. The defect may prevent X-ray imaging from starting or cause intermittent imaging when using the wired foot switch. Stop using the device immediately and follow recall instructions from Philips or your healthcare provider.

Philips Medical Systems Nederland B.V.
Philips has
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Health & Personal Care
HIGH
FDA DEVICE

Civco Medical eTRAX 14G Needle Sensor Recall for 5 Units (2026)

Civco Medical Instruments Co. is recalling 5 eTRAX Needle Sensor 14G units for Aurora Trackers. The recall cites a programming and inspection error that could cause the needle tip position to be misidentified on the user interface. Stop using the device immediately and contact Civco for instructions.

Civco Medical Instruments Co.
There was
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Health & Personal Care
HIGH
FDA DEVICE

Abiomed Purge Cassette Recall 2026: 33,107 Impella Pump Sets Worldwide Over Purge Leaks

Abiomed has issued a Class I recall for 33,107 Purge Cassette units used with Impella pump sets worldwide due to purge leaks in Generation 1 cassettes. The leaks raise the risk of compromised device performance. Patients and healthcare providers should stop using the affected devices immediately and follow Abiomed's recall instructions.

Abiomed
Increased risk
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Health & Personal Care
HIGH
FDA DEVICE

Medline Anterior Hip Pack Recall Affects 14,379 Kits With Olympus Biopsy Valves (2026)

Medline Industries, LP recalled 14,379 anterior hip pack kits distributed nationwide after Olympus biopsy valves showed rubber fragment detachment. The defect can release fragments into the patient’s airway, risking a foreign body in the tracheobronchial tree and prolonging procedures. Stop using the kit and follow recall instructions from Medline and your healthcare provider.

Medline
Kits contain
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Health & Personal Care
HIGH
FDA DEVICE

Merit Medical BioFlo DuraMax Catheter Recall 2026: 47,153 Units Worldwide

Merit Medical Systems recalled 47,153 BioFlo DuraMax Catheters distributed worldwide through medical distributors after a design defect in the 16F dual-valved splittable sheath introducer may fail to split as intended. The defect can cause hemorrhage, foreign bodies, and delays in procedures. Clinicians and patients should stop using the device immediately and follow recall instructions from Merit

Merit Medical Systems
16F dual-valved
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Health & Personal Care
HIGH
FDA DEVICE

Medtronic MiniMed 630G Insulin Pumps Recalled in 2026 for Insulin Delivery Errors (60,880 Units)

Medtronic MiniMed recalled 60,880 insulin pumps sold worldwide through healthcare providers and medical distributors, including the MiniMed 630G line. The defect is gravity related and can cause insulin over-delivery or under-delivery when the pump height changes relative to the infusion site. Patients should stop using the pumps immediately and follow recall instructions.

Medtronic MiniMed
All Medtronic
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Health & Personal Care
HIGH
FDA DEVICE

Burlington Medical Demi Half Aprons Recalled for Attenuation Degradation Risk (2026)

Burlington Medical recalled 29 Demi Half Aprons distributed worldwide after finding attenuation material may degrade over time. The degradation shortens the protective lifespan. Healthcare facilities should stop using the aprons immediately and follow the manufacturer’s recall instructions.

Burlington Medical
Potential for
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Tag Statistics

Total Recalls
35

Related Tags

electrical hazardback to schoolimmediate actionstop use immediatelyreturn for refundpoisoning risklithium batterygarageoutdoorplasticmetalfall hazard