Health & Personal Care Recalls

1,620 product recalls found in this category. Browse through all safety alerts and stay informed.

High Activity Category

This category has a significant number of recalls. Please check regularly for updates.

Health & Personal Care
HIGH
FDA DEVICE

Medline Puracol Collagen Wound Dressings Recalled for Elevated Endotoxin Levels (2026)

Medline recalled 108,971 units of Puracol MSC8522 and Puracol Plus MSC8622EP collagen wound dressings nationwide in the United States, with distribution to Mexico and Panama. Elevated endotoxin levels were identified in affected lots. Stop using the dressings and follow recall instructions provided by Medline or your healthcare provider.

Medline Industries, LP
Elevated endotoxin
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Health & Personal Care
HIGH
FDA DEVICE

Orthalign Lantern Knee Drill Plate Recalled for Bone-Cut Risk (2026)

Orthalign recalled 7 drill plates used with its Lantern Knee System distributed nationwide, including Utah. The parts were manufactured out of specification and can cause a bone cut up to 0.008 inch (2.8448 mm). Healthcare providers were notified by letter and instructions to stop using the devices.

Orthalign
Drill plates
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Health & Personal Care
HIGH
FDA DEVICE

Orthalign Drill Plate Recall 2026 for 7 Units Over Bone-Cut Risk

Orthalign recalled 7 pegged drill plates used with the Lantern Knee System due to out-of-spec manufacturing that can cause bone cuts up to 2.8448 mm. The devices were distributed in Utah and across the United States. Healthcare providers and patients should stop using the device immediately and await recall instructions by letter.

Orthalign
Drill plates
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Health & Personal Care
HIGH
FDA DRUG

LEO Pharma Recalls Adbry Injection Over Sterility Concerns

LEO Pharma Inc. recalled 11,407 units of Adbry injection on February 10, 2026. The recall stems from a lack of assurance of sterility due to particulate matter identified as wool fiber. Consumers should stop using the product immediately and contact their healthcare provider for guidance.

ADBRY
Lack of
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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 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 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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Health & Personal Care
HIGH
FDA DRUG

Fresenius Kabi Compounding Recalls Ketamine Injection for Sterility Risk

Fresenius Kabi Compounding recalled 1,410 bags of ketamine HCl injection on February 5, 2026. The recall stems from a lack of assurance of sterility, posing a high health risk. Healthcare providers and consumers must stop using this product immediately.

Fresenius Kabi Compounding
Lack of
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Health & Personal Care
HIGH
FDA DRUG

Fresenius Kabi Compounding Recalls Thiamine Injection Over Sterility Risk

Fresenius Kabi Compounding recalled 10,548 bags of thiamine HCl injection on February 5, 2026. The recall follows a lack of assurance of sterility, posing a high health risk. Affected products include several lots expiring between February and May 2026.

Fresenius Kabi Compounding
Lack of
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Health & Personal Care
HIGH
FDA DEVICE

Remel Recalls Campy CVA Medium Over Low Recovery Rates

Remel, Inc. recalled 97 units of Campy CVA Medium on February 5, 2026. Customers reported low to no recovery of Campylobacter Jejuni ATCC 33291 in the affected lot. Healthcare providers and patients must stop using the product immediately.

Remel
Customer complaints
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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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Health & Personal Care
HIGH
FDA DEVICE

GE Medical Systems Recalled 125 Imactis CT-Navigation System Stereotaxic Accessories in 2026

GE Medical Systems recalled 125 Imactis CT-Navigation System stereotaxic accessories distributed worldwide to healthcare facilities. The recall cites a potential mismatch between the simulated needle trajectory and the actual trajectory. Healthcare providers should stop using the devices immediately and follow the manufacturer's recall instructions.

GE Medical Systems
There is
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Health & Personal Care
HIGH
FDA DEVICE

B. Braun Medical 21GA Winged Infusion Set 7M2802 Recalled 51,300 Units (2026)

B. Braun Medical recalls 51,300 units of its 21GA Winged Infusion Set, model 7M2802, distributed worldwide including Texas and Costa Rica. The device’s needle tip can be dull or break, making advancement difficult. Stop using the device immediately and contact the manufacturer or your healthcare provider for instructions.

B. Braun Medical
The potential
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Health & Personal Care
HIGH
FDA DRUG

Pro Numb Tattoo Numbing Spray Recalled Due to cGMP Deviations

Pro Numb Tattoo Numbing Spray was recalled due to cGMP deviations. The recall affects products distributed nationwide in the USA. Consumers should stop using the spray immediately and contact Pro Numb Tattoo Numbing Spray LLC for guidance.

PRO NUMB
cGMP deviations
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Category Statistics

Total Recalls
1,620
Pages
81