stop use immediately Recalls

2,228 recalls tagged with “stop use immediately”.

Health & Personal Care
HIGH
FDA DEVICE

BD Kiestra ReadA Lab Automation Module Recalled in 2026 Over Connectivity Delays (82 Units)

BD Kiestra recalled 82 units of its ReadA lab automation module on February 6, 2026, including 7 in the United States and 65 overseas. The issue arises after a system reboot when one or more modules become unreachable via the remote connectivity interface, potentially delaying plate retrieval from the incubator. The problem is intermittent and did not affect test results, assay performance, or var

BD Kiestra Lab Automation
In certain
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Health & Personal Care
HIGH
FDA DEVICE

12 Million TRUE METRIX Blood Glucose Meters Recalled Due to E-5 Error Code Risk

Trividia Health recalled 12,067,458 TRUE METRIX blood glucose meters sold worldwide due to inadequate labeling. The manuals failed to emphasize that an E-5 error code could indicate a dangerously high blood glucose level. Users must stop using these devices immediately and contact their healthcare provider for further instructions.

Trividia Health
The system
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Health & Personal Care
HIGH
FDA DEVICE

Trividia Health TRUE METRIX PRO Owner's Booklet Recall for 1,001,534 Units (2026)

Trividia Health recalled 1,001,534 TRUE METRIX PRO owner’s booklets used with glucose meters distributed worldwide through multiple retailers. The labeling fails to clearly warn that an E-5 error could indicate very high blood glucose and does not emphasize immediate actions. Consumers should stop using the device and follow manufacturer recall instructions by letter, contacting Trividia Health or

Trividia Health
The system
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Health & Personal Care
HIGH
FDA DEVICE

International Life Sciences Recalls Artelon FLEXBAND TWIST Augmentation Devices for Endotoxin Test F

International Life Sciences issued an active recall of Artelon FLEXBAND TWIST augmentation devices. The devices were distributed worldwide, including nationwide in the United States. The recall concerns failures in bacterial endotoxin testing that could pose a infection risk; users should stop using the device and follow recall instructions from the manufacturer.

International Life Sciences
Augmentation devices
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Health & Personal Care
HIGH
FDA DEVICE

Trividia Health TRUE METRIX GO Recall for E-5 Error Misleading Labeling (1.4M, 2026)

Trividia Health's TRUE METRIX GO blood glucose kits sold at Walgreens, CVS and other retailers are recalled worldwide. The labeling fails to clearly emphasize that an E-5 error could indicate very high blood glucose and require immediate action. Consumers should stop using the device and follow manufacturer guidance.

Trividia Health
The system
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Health & Personal Care
HIGH
FDA DEVICE

Trividia Health Recalled 3.68 Million TRUE METRIX AIR Booklets for E-5 Error (2026)

Trividia Health recalled 3,678,026 TRUE METRIX AIR owner’s booklets distributed worldwide through Walgreens, CVS and other retailers. The recall centers on labeling for the E-5 error code, which could indicate very high blood glucose and lacks clear, immediate action guidance. Consumers should stop using the device and await manufacturer instructions mailed to customers.

Trividia Health
The system
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Health & Personal Care
HIGH
FDA DEVICE

International Life Sciences Recalls Artelon FlexBand Plus Augmentation Devices for Endotoxin Testing

International Life Sciences recalled Artelon FlexBand Plus augmentation devices after endotoxin testing failures. The recall affects devices with REF 41054 and REF 41057 distributed worldwide. Patients and healthcare providers must stop using the devices immediately and follow manufacturer instructions for recall return.

International Life Sciences
Augmentation devices
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Health & Personal Care
HIGH
FDA DEVICE

Hitachi Proton Beam Therapy Device Recalled for Software Issues

Hitachi Ltd. recalled one unit of its Proton Beam Therapy System on February 6, 2026 due to a software anomaly. The issue may result in positional discrepancies during patient treatment. The recall affects distribution in Texas and Washington D.C.

Hitachi, Ltd. Radiation Oncology Systems, Kashiwanoha
Software anomaly
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Health & Personal Care
HIGH
FDA DEVICE

Hitachi Proton Beam Therapy System Recalled Due to Software Issue

Hitachi recalled its Proton Beam Therapy System on February 6, 2026, due to a software anomaly that may result in positional discrepancies. The recall affects one unit distributed in Texas and Washington D.C. Healthcare providers and patients must stop using the device immediately.

Hitachi, Ltd. Radiation Oncology Systems, Kashiwanoha
Software anomaly
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Health & Personal Care
HIGH
FDA DRUG

Fresenius Kabi Vancomycin Injection Recalled Over Sterility Concerns

Fresenius Kabi Compounding recalled its vancomycin HCl injection on February 5, 2026, due to a lack of assurance of sterility. This Class II recall affects all lots distributed nationwide. Healthcare providers and consumers must stop using the product immediately.

Fresenius Kabi Compounding
Lack of
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Recalled Semfri Multi-Purpose Helmet - front view
HIGH
CPSC

Semfri Children's Helmets Recalled Over Serious Head Injury Risk

Semfri recalled children's helmets on February 5, 2026, due to safety violations. The helmets do not comply with mandatory safety standards, posing a serious risk of head injury. Consumers should stop using the helmets immediately and seek a refund.

Semfri Children's Helmets
The recalled
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Recalled GM Gumili Wintergreen Essential Oil-Bottle and Box Front
HIGH
CPSC

GM Gumili Wintergreen Essential Oil Recalled for Child Poisoning Risk

GM Gumili recalled its Wintergreen Essential Oil on February 6, 2026, after it was found to lack child-resistant packaging. The essential oil contains methyl salicylate, which poses a risk of poisoning to young children if ingested. Consumers should stop using the product immediately and return it for a full refund.

GM Gumili Wintergreen Essential Oil Bottles
The essential
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Recalled Lola + The Boys Candy Heart Tie Dye Set
HIGH
CPSC

Lola Plus The Boys Recalls 5 Youth Hoodies With Drawstrings Over Strangulation Risk (2026)

Lola Plus The Boys recalls five youth hooded clothing styles sold nationwide and online at Lolaandtheboys.com from November 2022 through September 2025. Drawstrings with beads on the recalled garments can snag on objects and pose a strangulation risk. Stop using the recalled clothing now and contact Lola Plus The Boys to obtain a full refund.

Lola Plus The Boys
The drawstrings
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Recalled PurSteam Elite Travel Steamer – Model PS-510
HIGH
CPSC

Aterian Recalls PurSteam Elite Travel Steamers and Mighty Lil Steamers for Burn Hazard (2026)

Aterian recalls PurSteam Elite Travel Steamers and PurSteam Mighty Lil Steamers sold after December 2020 due to a burn risk. The steamers can expel hot water from the steam nozzle during use. Affected consumers should stop using the recalled steamers and submit a recall request at recall.pursteam.com for a full refund, which requires cutting the cord and uploading a photo of the steamer with its C

Aterian
The steamers
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Recalled Kitosun Submersible LED Lights
HIGH
CPSC

Kitosun Submersible LED Lights Recalled Over Battery Ingestion Risk

Kitosun recalled Submersible LED Lights on February 5, 2026, due to a serious ingestion hazard. The lights contain accessible lithium batteries that pose a risk of internal chemical burns or death if ingested by children. Consumers should stop using the product immediately and return it for a full refund.

Kitosun Submersible LED Lights
The recalled
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Recalled Organic Zing Birch Essential Oil Bottle – in packaging
HIGH
CPSC

Organic Zing Birch Essential Oil Recalled Over Child Poisoning Risk

Organic Zing Birch Essential Oil bottles were recalled on February 5, 2026, due to poison risks for children. The essential oil contains methyl salicylate, which requires child-resistant packaging. The recall affects an undisclosed number of bottles sold online by Linkers.

Salvia Cosmeceuticals, of India
The essential
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Health & Personal Care
HIGH
FDA DRUG

Fresenius Kabi Compounding Issues Recall of Vancomycin Injection

Fresenius Kabi Compounding recalled 1,578 bags of vancomycin HCl injection on February 5, 2026. The company cited a lack of assurance of sterility as the reason for the recall. Healthcare providers and consumers should stop using the product immediately.

Fresenius Kabi Compounding
Lack of
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Tag Statistics

Total Recalls
2,228

Related Tags

electronicworkplaceimmediate actionreturn for refundelectrical hazardcpsc regulatedfda regulatedreplacement availablechemical hazardpoisoning riskbattery poweredadult product