glass Recalls

160 recalls tagged with “glass”.

Recalled Umeyda Shortsleeve Nightgown – Baby Pink Stripe
HIGH
CPSC

Umeyda Nightgowns Recalled for Burn Risk in 2025 Sold on Amazon

Umeyda recalled 100% cotton girls' nightgowns sold on Amazon. The recall involves nightgowns with a pocket and a front button closure. The garments do not meet mandatory flammability standards and pose a burn risk. Stop using them and email ameyda123@163.com for a full refund.

Umeyda
The recalled
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Health & Personal Care
HIGH
FDA DEVICE

GET TESTED INTERNATIONAL AB Biological Age & Longevity Test Recalled for Premarket Issue (3 Units,  

GET TESTED INTERNATIONAL AB recalled 3 units of the Biological Age & Longevity Test distributed nationwide in the United States. The recall concerns distribution without premarket approval or clearance. Consumers should stop using the device and follow the manufacturer's instructions. Contact GET TESTED INTERNATIONAL AB for guidance.

GET TESTED INTERNATIONAL AB
Distribution without
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Food & Beverages
HIGH
FDA FOOD

Blonde Beard's Dojo Asian Wing Sauce Recalled for Undeclared Soy (2025)

Blonde Beard's recalled 4,888 bottles of Dojo Asian Wing Sauce sold through multiple retailers in the United States and Canada after confirming undeclared soy on the label. The sauce is shelf-stable and packaged in 8-ounce glass bottles. Consumers should not consume the product and should contact Blonde Beard's for refund or replacement.

Blonde Beard's
Undeclared Soy
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Health & Personal Care
HIGH
FDA DEVICE

PHILIPS IntelliVue MP80 Recall 1,913,441 Monitors Worldwide for Alarm Failure (2025)

Philips North America LLC recalled 1,913,441 IntelliVue MP80 patient monitors distributed worldwide to hospitals after reports the devices did not alarm. The defect could prevent alarms from sounding in critical patient situations. Healthcare facilities should stop using the monitors and follow recall instructions from the manufacturer.

Philips
Potential issue
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Health & Personal Care
HIGH
FDA DRUG

Nivagen Zinc Oxide Ointment Recall 912 Containers Over cGMP Deviations (2025)

Nivagen Zinc Oxide Ointment 20% skin protectant, manufactured in India for Nivagen Pharmaceuticals and distributed nationwide in the USA, is recalled. The recall covers 912 containers. The defect cited is cGMP deviations. Consumers and healthcare providers should stop using the product and follow guidance from Blossom Pharmaceuticals or a healthcare professional.

Nivagen Zinc Oxide
cGMP deviations
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Health & Personal Care
HIGH
FDA DEVICE

Siemens MAMMOMAT Fusion Operator Table Recalled for Bus-Installation Risk (2025)

One unit of the Siemens MAMMOMAT Fusion operator table is recalled after being sold with a bus-installation kit. The device is not intended for bus installations and is designed for stationary operation. Health care providers should stop using the device immediately and follow the manufacturer’s recall instructions.

Siemens Medical Solutions USA
There were
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Health & Personal Care
HIGH
FDA DEVICE

Medtronic MiniMed CareLink Clinic Recall 12,126 Units Worldwide in 2025

Medtronic MiniMed recalled 12,126 CareLink Clinic units worldwide after a software error misdisplays the 24-hour Sensor Glucose Overview Graph. The faulty software could prompt clinicians and patients to make therapy decisions based on incorrect glucose data. Patients should stop using the device immediately and contact Medtronic MiniMed or their healthcare provider for instructions.

Medtronic MiniMed
Software error
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Recalled RH Byron Reeded Stone Dining Table in Italian Classico Travertine
MEDIUM
CPSC

RH Byron Tables and Desks Recalled for Injury Risk — 31 SKUs in 2025

RH recalled Byron tables and desks sold at RH Galleries and outlets and on RH.com from November 2023 through July 2025. The recall covers 31 SKUs across three models with stone and marble tops and wood legs. The recalled furniture can collapse if a gap forms between the leg and tabletop and a horizontal force is applied. Consumers should stop using recalled units and contact RH for a full refund,,

RH
The recalled
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Recalled Yamaha Drive 2 J0D/J0E/J5C
HIGH
CPSC

Yamaha Recalls 2021-2025 Drive 2 Golf Cars for Crash Hazard With No Stop Lights

Yamaha recalls 2021-2025 Drive 2 PTV golf cars sold by Yamaha dealers nationwide between June 2020 and July 2025. The recalled golf cars lack stop lights, creating a crash hazard that could result in serious injury or death. Owners should stop using the recalled golf car immediately and contact an authorized Yamaha Golf Car dealer for a free installation of two stoplights.

Yamaha
The recalled
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Recalled E-Z-GO Valor PTV
HIGH
CPSC

Textron E-Z-GO Recalls Personal Transportation Vehicles Over Fuel Leak Fire Hazard (2025)

Textron E-Z-GO recalled certain personal transportation vehicles due to a fuel-line leak that can spark a fire. The recall covers RXV Freedom and Valor PTVs from model years 2020-2025 and TXT Freedom and Valor PTVs from model years 2020-2022. Dealers will inspect and replace the fuel line at no cost, and owners should stop using the vehicles until inspected.

Textron E-Z-GO
The recalled
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Health & Personal Care
HIGH
FDA DEVICE

Glycar SA Recalls 18 SJM Pericardial Patch EnCap 5x10 cm REF C0510 in 2025 Recall

Glycar SA recalls 18 SJM Pericardial Patch with EnCap Technology 5x10 cm distributed in the US to healthcare facilities. The lot may not meet the required tensile strength specification. Stop use and follow manufacturer instructions provided by Glycar and your healthcare provider. Notification was issued by email.

Glycar SA
The impacted
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Food & Beverages
HIGH
FDA FOOD

Food Club Finely Shredded Pizza Style Four Cheese Blend Recalled for Metal Fragments in 117 Cases (-

Food Club recalled 117 cases of Finely Shredded Pizza Style Four Cheese Blend, sold at multiple retailers nationwide, after potential metal fragments were found in a supplier raw material. The 8-ounce packages contain mozzarella, provolone, parmesan and romano cheeses and carry UPC 3680017231. Consumers should not eat this product and should contact Great Lakes Cheese Co for refund or replacement.

Food Club
Potential metal
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Health & Personal Care
HIGH
FDA DRUG

Camber Ketorolac Tromethamine Injection Recall 2025 for Glass Particulates

Camber Pharmaceuticals recalled Ketorolac Tromethamine Injection, USP, 60 mg/2 mL, 2 mL single-dose vials distributed nationwide in the United States. The recall is due to the presence of glass particulates. Healthcare providers and patients should stop using the product immediately and contact Aspiro Pharma Limited at 1-866-495-1995 for guidance.

Ketorolac Tromethamine
Presence of
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Health & Personal Care
HIGH
FDA DRUG

Medline 222,800 Alcohol Prep Pads Recalled for Subpotent Drug (2025)

Medline Industries recalled 222,800 alcohol prep pads nationwide on Sept. 29, 2025 due to subpotent potency. The pads are 2-ply, 70% isopropyl alcohol. Stop using immediately and contact Medline or your healthcare provider for guidance.

Medline Industries
Subpotent Drug
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Food & Beverages
HIGH
FDA FOOD

Wholesale Produce Supply LLC Recalls 307 Cases of Cut Fresh Fruit Mix for Listeria Risk (2025)

Wholesale Produce Supply LLC recalls 307 cases of Cut Fresh Fruit Mix sold through multiple retailers in Iowa, Illinois, North Dakota, Nebraska and Wisconsin. The recall covers two brand variations and multiple lot numbers with October 2025 expirations. Consumers should not consume the product and should contact Wholesale Produce Supply LLC DBA for refund or replacement information.

Wholesale Produce Supply LLC
Potential Listeria
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Food & Beverages
HIGH
FDA FOOD

Albertsons Recalls Store-Made Ready Meals Pesto Bowtie Pasta Salad Over Listeria (2025)

Albertsons recalled store-made Ready Meals Pesto Bowtie Pasta Salad sold at banners including Albertsons, Pavilions, Randalls, Safeway, Tom Thumb and Vons. The recall concerns a bowtie pasta ingredient contaminated with Listeria monocytogenes. Do not consume the product and seek a refund or replacement from Albertsons Companies LLC.

Albertsons
Listeria monocytogenes.
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