toddler product Recalls

37 recalls tagged with “toddler product”.

Health & Personal Care
HIGH
FDA DEVICE

Reflexion Medical Recalls 12 RefleXion X1 Radiotherapy Systems for Software Defect (2026)

Reflexion Medical recalled 12 RefleXion X1 Radiotherapy System RXM1000 units sold to hospitals and healthcare providers in the United States after a software defect could cause a 5mm or greater misalignment and underdose. The defect occurs during angular roll corrections followed by a repeat localization, and the roll corrections from the initial localization are not carried through to treatment.

Reflexion Medical
Due to
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Food & Beverages
HIGH
FDA FOOD

Mangalm Tops GOLD Mixed Pickle Recalled for Erucic Acid Adulteration Risk (2026)

Mangalm LLC recalled Tops GOLD Mixed Pickle sold in California, Nevada, Oregon, Utah and Washington after FDA enforcement. The product may be adulterated with erucic acid from mustard oil. Consumers who purchased it should not eat it and should contact Mangalm for refund or replacement via email.

Mangalm
Potential adulteration
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Health & Personal Care
HIGH
FDA DEVICE

I.T.S. Pelvic Reconstruction System Recall for MRI Heating Risk (46,637 Units) 2026

I.T.S. recalled 46,637 pelvic reconstruction system components nationwide in the United States after MRI safety testing showed higher RF-induced heating than the IFU stated. The issue centers on MRI heating under certain conditions that could injure patients. Patients should stop using the devices and follow manufacturer recall instructions.

I.T.S. GmbH
Updated MRI
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Health & Personal Care
HIGH
FDA DEVICE

I.T.S. GmbH LRS Orthopedic System Recall: 176 Units for MRI Heating Risk (2026)

ITS GmbH recalled 176 units nationwide in the United States after MRI safety testing showed higher RF-induced temperature increases under certain MRI conditions. The issue could cause burns during MRI exposure. Healthcare providers and patients should stop using the device immediately and follow recall instructions.

I.T.S. GmbH
Updated MRI
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Health & Personal Care
HIGH
FDA DEVICE

ITS GmbH Recalled 510 I.T.S Straight Plate with Angular Stability Over MRI Heating Risk (2026)

ITS GmbH recalled 510 units of the I.T.S Straight Plate with Angular Stability after MRI safety testing showed higher RF-induced temperature increases under certain MRI conditions. The recall covers multiple article numbers across forearm and straight plates and distributions nationwide in the United States. No injuries or incidents have been reported at this time. Healthcare providers andpatients

I.T.S. GmbH
Updated MRI
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Health & Personal Care
MEDIUM
FDA DRUG

Green Guard Antiseptic Wipes Recall 2026 Over CGMP Deviations

Green Guard Antiseptic Wipes, distributed nationwide by ACME United Corporation, are being recalled as of January 20, 2026. FDA enforcement cites CGMP deviations in manufacturing for the benzalkonium chloride wipes, NDC 47682-056-73. Consumers and healthcare providers should stop using the product immediately and contact ACME United for guidance on refunds or replacements.

Green Guard Antiseptic Wipes
CGMP Deviations
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Health & Personal Care
HIGH
FDA DRUG

Medi-First Antiseptic Wipes Recalled for CGMP Deviations in 2026, 100 Wipes per Box

ACME United Corporation recalled Medi-First Antiseptic Wipes sold nationwide in the United States. The recall cites CGMP deviations that could affect product quality. Consumers and healthcare providers should stop using the wipes immediately and contact ACME United Corporation or a healthcare provider for guidance.

Medi-First Antiseptic Wipes
CGMP Deviations
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Health & Personal Care
HIGH
FDA DRUG

Dynarex BZK Antiseptic Towelettes 100-Count Recalled for CGMP Deviations (2026)

Dynarex recalled 100-pack BZK Antiseptic Towelettes sold nationwide after FDA enforcement cited CGMP deviations. The recall covers multiple lots, including Lot 52347-R, 52348-R, 52349-R, 52350, 52351-R, 52352, Exp. Date Mar 2027 and Exp. Date Jun 2027. Consumers should stop using the product immediately and contact ACME UNITED CORPORATION or their healthcare provider for guidance.

Dynarex
CGMP Deviations
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Health & Personal Care
HIGH
FDA DRUG

Cipla Lanreotide Acetate Injection Recall: 15,221 Syringes Over Particulate Matter (2026)

Cipla USA, Inc. is recalling 15,221 Lanreotide Acetate Injection syringes nationwide in the United States after detecting particulate matter. The defect is the presence of particulate matter in the injectable solution. Healthcare providers and patients should stop using the product immediately and contact Cipla USA for guidance.

LANREOTIDE ACETATE
Presence of
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Health & Personal Care
HIGH
FDA DRUG

GOLD STAR DISTRIBUTION LIQUID NYQUIL Recall 12/8oz Bottles 2026

GOLD STAR DISTRIBUTION recalls LIQUID NYQUIL regular and cherry 12/8oz bottles nationwide in the United States. The recall cites CGMP deviations and insanitary conditions including rodent exposure at the distribution center. Consumers should stop using the product immediately and contact Gold Star Distribution Inc for guidance on refunds or replacements.

GOLD STAR DISTRIBUTION
CGMP Deviations:
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Recalled Meaicezli Play Purse Set Packaging
HIGH
CPSC

Meaicezli Play Purse Sets Recalled Over Battery Ingestion Risk

Meaicezli recalled Play Purse Sets on December 18, 2025, due to a risk of serious injury from battery ingestion. The toys contain button cell and lithium coin batteries accessible to children. Consumers must stop using the products and return them for a full refund.

Meaicezli
The children's
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Recalled SKCAIHT Children's Mermaid Costume
HIGH
CPSC

SKCAIHT Recalls Children's Costumes Over Phthalate Exposure Risk

SKCAIHT recalled children's mermaid costumes on December 11 due to a risk of injury from phthalate exposure. The costumes, sold on Amazon, violate federal regulations concerning toxic substances. Consumers should stop using the costumes immediately and seek a refund.

SKCAIHT Children's Costumes
The children's
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Vehicles & Parts
HIGH
NHTSA

Nissan Recalls 2025 Kicks Over Rollaway Risk

Nissan North America recalled certain 2025 Kicks vehicles on November 12, 2025, due to a malfunctioning "Shift-to-Park" warning. The issue may lead to unexpected vehicle movement when the ignition is shut off while not in park, posing a rollaway risk. Owners will receive notification letters with further instructions, including a free fix.

Nissan
When the
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Infant side of Recalled Modera Organic Cotton Pack N Play Mattress Dual-Sided Portable Baby Crib Pad
HIGH
CPSC

Modera Recalls Pack N Play Mattresses Over Entrapment Risk

Modera recalled Pack N Play mattresses on October 30, 2025, due to serious entrapment hazards. These mattresses may not fit securely in play yards, risking suffocation. Consumers must stop using the mattresses and contact Modera for refunds.

Modera
The after-market
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Health & Personal Care
HIGH
FDA DEVICE

Baxter Healthcare Recalls IV Extension Sets Over Leak Risk

Baxter Healthcare recalled 15,552 IV extension sets on August 29, 2025, due to a leak risk. The recall affects products distributed nationwide across 50 states. Healthcare providers and patients must stop using the devices immediately.

Baxter Healthcare
IV sets
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Tag Statistics

Total Recalls
37

Related Tags

immediate actionstop use immediatelyreturn for refundadult productelderly productelectrical hazardlithium batterycpsc regulatedfda regulatednhtsa regulatedelectronicreplacement available