living room Recalls

50 recalls tagged with “living room”.

Health & Personal Care
HIGH
FDA DEVICE

Siemens Medical Solutions USA Recalls MAMMOMAT Inspiration Operator Table for Bus-Installation Risk

Siemens Medical Solutions USA recalls the MAMMOMAT Inspiration operator table. The recall covers six units worldwide, including three in the United States. The operator table was sold with a bus-installation kit and is not designed or released for bus installations. Stop using the device immediately and contact Siemens for instructions.

Siemens Medical Solutions USA
There were
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Recalled Sauna Model Tylö Halmstad 2
MEDIUM
CPSC

Sauna360 Recalls Tylö Halmstad and Kiruna Hybrid Saunas Over Fall Hazard

Sauna360 recalls Tylö Halmstad and Kiruna Hybrid saunas sold by Sauna360 distributors nationwide from July 2024 through December 2024 for between $6,000 and $12,000. The recall targets bench seating that can collapse, creating a fall hazard. Stop using the benches immediately and contact Sauna360 for a free repair.

Sauna360
The saunas
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Recalled Cranach Hardware Plastic Tip Restraint Kit
HIGH
CPSC

Cranach Hardware Recalls Tip Restraint Kits for Tip-Over Hazard (2025)

No injuries have been reported. Cranach Hardware recalled tip restraint kits sold through retailers after testing showed the plastic brackets and tie can fail to meet safety standards. Stop using the restraints and contact Cranach Hardware for a free stainless steel replacement kit.

Cranach Hardware
The recalled
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Recalled Persilux Zebra Blinds
HIGH
CPSC

Persilux Zebra Blinds Recalled for Strangulation Risk, Sold on Amazon

Persilux recalled zebra blinds sold on Amazon after safety hazards were found. The recall cites long operating cords that can cause strangulation and entanglement. The company offers a free repair kit and instructions to remove cords. Consumers should stop using the product immediately and contact Persilux for remedy information.

Persilux
The recalled
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Food & Beverages
HIGH
FDA FOOD

Southwind Foods' Tovala-brand Frozen Shrimp Recalled for Cs-137 Contamination (93,122 Cases, 2025)

Southwind Foods LLC, doing business as Great American Seafood Imports, recalled 93,122 cases of Tovala-brand frozen raw phosphate-free shrimp after identifying potential Cesium-137 contamination. The recall expands a prior action and notes insanitary production conditions. Consumers who bought the 5 oz IQF bag with UPC 829944085788 should not eat it and should contact the supplier for refund or re

Southwind Foods LLC dba Great American Seafood Imports
Product manufactured
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Food & Beverages
HIGH
FDA FOOD

Black Sheep Egg Company Recalls 58,500 Dozen Free Range Eggs for Salmonella Risk (2025)

Black Sheep Egg Company recalls 58,500 dozen free range Grade AA medium brown eggs after FDA enforcement notice citing potential Salmonella contamination. The recall covers eggs sold in Arkansas and Missouri, with wholesale and broker locations in Mississippi, Texas, California and Indiana. Consumers should not eat these eggs and should contact Black Sheep Egg Company for refund or replacement.

Black Sheep Egg Company
Potential Salmonella
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Health & Personal Care
HIGH
FDA DRUG

Glenmark Azelaic Acid Gel Recall Affects 13,824 Tubes Sold Nationwide in 2025

Glenmark Pharmaceuticals Inc. USA recalls 13,824 tubes of azelaic acid gel 15% after CGMP deviations prompted gritty texture complaints. The recall covers nationwide distribution in the United States. Consumers should stop using the product and contact Glenmark for guidance.

Glenmark Pharmaceuticals
CGMP Deviations:
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Health & Personal Care
HIGH
FDA DEVICE

Olympus BF-PE2 Bronchoscope Recall Expands with 4,289 Units Aboard Outside US

Olympus Corporation of the Americas confirms a Class I recall of the BRONCHOFIBERSCOPE BF TYPE PE2. The recall covers 2 units in the US and 4,289 units outside the US. Updated IFU guidance aims to clarify safe use with laser, argon plasma coagulation and high-frequency therapy equipment.

Olympus Corporation of the Americas
Additional IFU
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Health & Personal Care
HIGH
FDA DEVICE

Philips Allura Xper FD10 Recalled for BIOS Battery Startup Failure (2,317 Units Worldwide, 2025)

Philips Medical Systems Nederland recalled 2,317 Allura Xper FD10 imaging systems worldwide, including 497 in the United States. The BIOS battery may deplete faster than expected, causing the startup process to halt with no user alerts. Hospitals should stop using the devices and await manufacturer instructions.

Philips Medical Systems Nederland
The BIOS
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Health & Personal Care
HIGH
FDA DEVICE

Baxter Healthcare Recalls 136,512 CLEARLINK IV Sets DUO-VENT for Leak Risk (2025)

Baxter Healthcare recalled 136,512 CLEARLINK System Solution Set DUO-VENT IV sets distributed nationwide in the United States after detecting a leak risk. The Luer Activated Valve design may leak, potentially compromising IV administration. Hospitals and patients should stop using the device immediately and follow Baxter recall instructions.

Baxter Healthcare
IV sets
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Health & Personal Care
HIGH
FDA DRUG

Ascend Laboratories Recalls ARIPIPRAZOLE 10 mg Tablets Over Superpotent Drug Risks (2025)

Ascend Laboratories, LLC recalls 2,256 bottles of ARIPIPRAZOLE 10 mg tablets distributed nationwide after discovering the product to be superpotent. The recall involves ARIPIPRAZOLE tablets manufactured by Alken Laboratories Ltd. in India and distributed in the United States. The recall date is August 28, 2025, with consumer notification by letter and guidance to stop use.

ARIPIPRAZOLE
Superpotent drug
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Food & Beverages
HIGH
FDA FOOD

Sunrise Creamery Dilly Pickle Monterey Jack Cheese Recalled Over Listeria Risk (2025) by Middlefield

Sunrise Creamery Monterey Jack Cheese with Dill Pickles is recalled by Middlefield Original Cheese Cooperative after FDA findings indicate potential Listeria monocytogenes contamination. The recall covers two SKUs in 6 oz and 1.25 lb sizes, distributed to Ohio, Pennsylvania, Wisconsin and Texas. Consumers should discard affected cheese and contact the cooperative for refund or replacement.

Sunrise Creamery
Potential contamination
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Recalled LED module
HIGH
CPSC

Viewrail Recalls LED Control Module for Floating Stairs Over Fire Hazard

Viewrail recalls the electronic LED module E2-WR used with floating stairs and rails after a fire hazard was identified. The recall covers modules located inside the metal stringer tube at the back of the stairs. The recall was announced by the CPSC on 2025-08-14. Consumers should stop using the module and contact Viewrail for a replacement or refund.

Viewrail
The LED
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Tag Statistics

Total Recalls
50

Related Tags

immediate actionreturn for refundelectrical hazardtip over riskfederal law violationcpsc regulatedmandatory standard violationinfant productadult productpet relatedkitchenbathroom
    living room Recalls | RecallRadar