mandatory standard violation Recalls

147 recalls tagged with “mandatory standard violation”.

Health & Personal Care
HIGH
FDA DEVICE

Burlington Medical Recalled 15,438 Radiation Attenuation Vests Over Degradation Risk (2026)

Burlington Medical recalled 15,438 attenuation vests distributed worldwide after potential attenuation degradation over time. The vests use Xenolite 800 attenuation material and were produced between January 16, 2025 and January 21, 2026. Healthcare providers and patients should stop using the vest immediately and follow recall instructions.

Burlington Medical
Potential for
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Health & Personal Care
HIGH
FDA DEVICE

Burlington Medical Blockers Recalled for Attenuation Degradation in 51 Units Worldwide (2026)

Burlington Medical recalled 51 Blocker devices sold worldwide after a recall notice. The devices may degrade attenuation over time, shortening their lifespan. Stop using the devices immediately and follow the manufacturer’s recall instructions. Contact Burlington Medical, LLC or your healthcare provider for guidance. Distribution is worldwide.

Burlington Medical
Potential for
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Recalled Fixwal 7- drawer dresser (front)
HIGH
CPSC

Fixwal 7-Drawer Dressers Recalled Over Tip-Over Hazard

Fixwal recalled its 7-Drawer Dressers on February 5, 2026. The dressers pose severe tip-over and entrapment hazards, particularly to children. Consumers should immediately stop using these furniture units and seek a refund.

Fixwal 7-Drawer Dressers
The recalled
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Recalled Shintenchi 6-Drawer Dresser, model SHX12077-WH (front)
HIGH
CPSC

Shintenchi Dressers Recalled Due to Tip-Over Hazard

Shintenchi recalled 30,000 6-drawer dressers on February 5, 2026. The dressers pose a serious tip-over and entrapment risk to children if not anchored to the wall. Consumers should stop using the dressers immediately and seek a refund.

Huizhou Sunhouse Home Furnishings Co., Ltd., of China
The recalled
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Recalled LOTUSJOY Sweet Birch Essential Oil - Packaging, Bottle and Glass Dropper
HIGH
CPSC

Zan International Trading Recalls Lotus Joy Sweet Birch Essential Oil Packaging (2026)

Zan International Trading recalls Lotus Joy Organic Sweet Birch Essential Oil bottles due to packaging that is not child-resistant. The product contains methyl salicylate and poses a poisoning risk to children if swallowed. Stop using the product now and return it for a full refund by contacting Zan International Trading.

Zan International Trading
The essential
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Recalled Scepter B62 Gas and Oil Fuel Container – front
HIGH
CPSC

Scepter B62 Gas and Oil Fuel Containers Recalled for Flash Fire Risk (2026)

Scepter B62 dual-chamber fuel containers imported by Mameix Retail are recalled for a flash fire and child poisoning risk. The recall cites a lack of flame-mitigation devices and a non–child-resistant spout. Consumers should stop using the recalled containers and contact Mameix Retail for a full refund.

Scepter
The recalled
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Health & Personal Care
HIGH
FDA DEVICE

Exactech Equinoxe Core Instrument Kit KIT-311X Recalled for Missing Cross-Pin

Exactech recalls 596 Equinoxe Core Instrument Kit units due to a missing cross-pin on the impacter handle. The alert, categorized as a Class II recall, was issued Feb 3, 2026 and remains active. Affected kits were distributed across the United States and in multiple international markets. Stop using the device and follow manufacturer instructions for recall remedies.

Exactech
Impactor handle
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Recalled Bazic Silicone Glue – Front and Side
HIGH
CPSC

Bazic Products Recalls Silicone Glue Over Child Poisoning Risk

Bazic Products recalled Bazic Silicone Glue on January 29, 2026, due to a serious poisoning risk for children. The glue's packaging does not meet child-resistant standards, violating federal law. Consumers should stop using the product immediately and seek a full refund.

Bazic Products
The glue
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Health & Personal Care
HIGH
FDA DRUG

Teva Metoprolol Succinate 50 mg Extended-Release Recall 2026 Following Failed Dissolution Specs (67,

Teva Pharmaceuticals recalled 67,043 bottles of Metoprolol Succinate Extended-Release Tablets, 50 mg, distributed nationwide. The FDA enforcement report cites Failed Dissolution Specifications as the hazard. Health care providers and patients should stop using this product immediately and contact Teva for guidance.

METOPROLOL SUCCINATE
Failed Dissolution
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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 Yetonamr Pull String Teething Toy – blue
HIGH
CPSC

Yetonamr Pull String Teething Toys Recalled Due to Choking Hazard

Yetonamr recalled Pull String Teething Toys on January 22, 2026, due to choking risks. The toys violate safety standards with silicone strings that can obstruct breathing. Consumers must stop using the toys immediately and seek refunds.

Yetonamr Pull String Teething Toys
The recalled
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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 DRUG

Med Nap Cleansing Towelettes Recall Expanded Over CGMP Deviations (2026)

ACME United Corporation recalls Med Nap Cleansing Towelettes, 5"x7" Benzalkonium Chloride 0.13%, distributed nationwide. CGMP Deviations prompted the recall. Stop using the product now and contact ACME United or a healthcare provider for guidance.

MED NAP CLEANSING TOWELETTE
CGMP Deviations
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Health & Personal Care
HIGH
FDA DEVICE

GE Healthcare Centricity Universal Viewer ZFP Recall 250 Units Worldwide in 2026

GE Healthcare recalled 250 Centricity Universal Viewer Zero Footprint Client units distributed worldwide after finding a risk that patient information may not match displayed images in certain workflows. The issue affects ZFP v6.0 SP11.6, SP11.6.0.1 and SP11.6.1 when Patient Timeline is installed. Hospitals should stop using affected units and await instructions from GE Healthcare.

GE Healthcare
Under certain
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Recalled Asher Pajama Set
HIGH
CPSC

Morgan Lane Recalls Children's Pajama Sets Over Burn Hazard

Morgan Lane recalled Asher Pajama Sets on January 15, 2026, due to a burn hazard. The pajamas do not meet mandatory flammability standards for children's sleepwear. Consumers should stop using the pajamas immediately and request a refund.

Morgan Lane
The recalled
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Health & Personal Care
HIGH
FDA DEVICE

Waldemar Link Endo-Model Replacement Plateau Recall for Detachment Risk (2026)

Waldemar Link recalled 1 unit of Endo-Model Replacement Plateau worldwide, including the United States in New Jersey. The device could detach its bushing from the screw shaft because of a longitudinal fracture. Clinicians and patients should stop using the device and await manufacturer instructions.

Waldemar Link GmbH & Co. KG
The potential
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Tag Statistics

Total Recalls
147

Related Tags

immediate actionstop use immediatelyreplacement availablereturn for refundfda regulatedcpsc regulatedpoisoning riskadult productnhtsa regulatedinfant productholiday productplastic