toddler product Recalls

292 recalls tagged with “toddler product”.

Health & Personal Care
HIGH
FDA DEVICE

Medline NAMIC Angiographic Rotating Adaptor Syringes Recalled in Class I Action for 79,843 Units

Medline Industries issued a Class I recall for 79,843 medical convenience kits containing NAMIC Angiographic Rotating Adaptor syringes. The action covers worldwide distribution including the US and PR. The risk is a syringe adaptor unwinding during use, which may cause a loose connection or disconnection with the manifold. Stop using the device immediately and follow recall instructions.

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

Spacelabs Healthcare 91496 Multi-parameter Module Recall Affects 1,790 Units Worldwide (2026)

Spacelabs Healthcare recalled the Multi-parameter Command Module, Model 91496, optioned with Masimo or Nellcor, distributed worldwide. A circuit board issue in Auto mode may trigger CO readings improperly, causing Bad Curve or Irregular Curve errors. Stop using immediately and follow manufacturer instructions.

Spacelabs Healthcare
Multi-parameter command
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Health & Personal Care
HIGH
FDA DEVICE

Medline NAMIC Angiographic Rotating Adaptor Syringes Recalled in 2,980 Kits Worldwide

Medline Industries, LP recalls 2,980 medical convenience kits containing NAMIC Angiographic Rotating Adaptor syringes. The recall spans the United States, Puerto Rico and multiple international countries. The rotatable adaptor may unwind during use, risking a loose connection or disconnection between syringe and manifold. Patients and healthcare providers should stop using the device and followMed

Medline Industries, LP
Medline Industries,
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Food & Beverages
HIGH
FDA FOOD

American Laboratories Pepsin Full Strength Powder Recalled for Salmonella Contamination (400 kg, 202

American Laboratories recalled 400 kg of Pepsin Full Strength Powder sold to 11 direct wholesale accounts in AZ, CA, FL, MO, NM, OH, SC, UT, WI and one wholesale account in Australia after a recall cited potential Salmonella contamination. The product is Item #5000545 and packed in double poly-lined drums or boxes. Consumers should not consume this product and should contact American Laboratories,

American Laboratories
Potential Salmonella
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Health & Personal Care
HIGH
FDA DEVICE

Olympus PKS Cutting Forceps 920000PK Recalled Worldwide in 2026 for Welding Defects

Olympus recalls 7 PKS Cutting Forceps worldwide because welded components may fail. The devices are used with a 5mm cannula and an electrosurgical generator. Stop using the device and follow the manufacturer’s recall instructions. Healthcare facilities should verify device details and consult Olympus for replacement options.

Olympus Corporation of the Americas
Olympus identified
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Food & Beverages
HIGH
FDA FOOD

Novamex Coconut Water Recall Targets 12,000 Cases Over Packaging Nutrition Facts Discrepancy

A Tipp Distributors, Inc. dba Novamex recall affects 12,000 cases of C2O Coconut Water with Pulp sold across multiple states. The outer cardboard box lists an incorrect Nutrition Facts Panel and Ingredient List, omitting added sugar. The can itself has the correct information. Consumers should avoid consumption and seek refund or replacement.

Novamex
The outer
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Recalled Christmas-themed Magnetic Chess Game - packaging
HIGH
CPSC

Magnetic Chess Games Recalled Due to Serious Injury Risk

Yiruikeji2024 recalled magnetic chess games on February 24, 2026, due to ingestion hazards. The games contain loose magnets that can pose serious health risks to children. Consumers should stop using the product and seek a refund immediately.

Magnetic Chess Games
The recalled
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Food & Beverages
HIGH
FDA FOOD

Made Fresh Salads Recalls 557 Tofu Whipped 5-lb Tubs Over Listeria Contamination (2026)

Made Fresh Salads recalled 557 five-pound tubs of Tofu Whipped sold in New York after an FDA notice identified possible Listeria monocytogenes contamination. The recall cites a risk to consumer safety. Consumers who bought the product should not consume it and should contact Made Fresh Salads Inc for refunds or replacements by telephone.

Made Fresh Salads
Products may
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Health & Personal Care
HIGH
FDA DEVICE

XTANT Medical Xpress Pedicle Screw System Dual Lead 6.5 x 50 mm Recalled for Mislabeling of Screw S

XTANT Medical Holdings recalls 2 units of the Xpress Pedicle Screw System Dual Lead 6.5 x 50 mm due to mislabeled lot that misidentifies screw length. The recall affects units distributed in the US, specifically Oregon. Healthcare providers and patients should stop using the device immediately and follow manufacturer instructions for recall actions.

XTANT Medical Holdings
Units from
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Health & Personal Care
HIGH
FDA DEVICE

Molded Products MPC-130 See Luer Cap Set Recalled for High-Risk Assembly Issue (2026)

Molded Products recalled 26,900 MPC-130 See Luer Cap Sets used in intravascular administration nationwide in the United States. The recall is active as of 2026-04-15. The threaded sleeve may not engage and can detach. Health risk is high. Stop using the device and follow the manufacturer’s recall instructions.

Molded Products
Molded Products,
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Health & Personal Care
HIGH
FDA DEVICE

Medline Recalls 14,379 Olympus Biopsy Valve Kits in 2026

Medline Industries, LP recalled 14,379 kits nationwide that include Olympus biopsy valves. The recall concerns rubber fragments detaching in the slit of single-use biopsy valves. Stop using these kits immediately and follow manufacturer instructions for return or replacement.

Medline
Kits contain
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Health & Personal Care
HIGH
FDA DEVICE

Medline Recalls 14,379 Olympus Biopsy-Valve Kits in 2026

Medline Industries is recalling 14,379 kits nationwide that include Olympus biopsy valves. The recall follows reports of rubber fragments detaching from the valves during use. Healthcare providers and patients should stop using the affected kits and follow Medline’s recall instructions.

Medline Industries, LP
Kits contain
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Health & Personal Care
HIGH
FDA DEVICE

Medline Airway Exam Kit Recalled for 14,379 Units Over Olympus Valve Detachment (2026)

Medline Industries, LP recalled 14,379 Airway Exam Kits containing Olympus biopsy valves nationwide. The recall cites rubber fragments detaching from the slit of single-use biopsy valves. Potential harm includes a foreign body in the patient’s tracheobronchial tree, inflammatory response, hypoxia, and longer procedures. Providers and patients should stop using the kit and follow recall directions.

Medline Industries, LP
Kits contain
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Health & Personal Care
HIGH
FDA DEVICE

Medline ENFIT G-Tube Connector ENFIT1010GC Recalled for Leakage Risk (651,789 Units, 2026)

Medline Industries recalled 651,789 ENFIT G-TUBE connectors (ENFIT1010GC) sold worldwide, including the United States and Canada. The connectors were not manufactured to required dimensional specifications and may not seal properly with ENFit-style devices, which could lead to leakage. Healthcare facilities and patients should stop using this device immediately and follow recall instructions from

Medline Industries
Connectors were
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Health & Personal Care
HIGH
FDA DEVICE

Medtronic MiniMed Paradigm Veo Insulin Pump Recalled for 55,724 Units (2026)

Medtronic MiniMed recalls 55,724 Paradigm REAL-Time Veo insulin pumps distributed worldwide. The pumps can deliver too much insulin when raised or too little when lowered relative to the infusion site due to gravity-driven pressure changes. Patients should stop using the device and contact Medtronic MiniMed or their healthcare provider for instructions and refunds.

Medtronic MiniMed
All Medtronic
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Health & Personal Care
HIGH
FDA DEVICE

Erbe USA Recalls 2,408 Flexible Cryoprobes for Surgery Over Rupture Risk (2026)

Erbe USA recalled 2,408 Flexible Cryoprobes (REF 20402-411) used in surgery nationwide, including Puerto Rico. Probes may rupture or burst during activation. Hospitals and healthcare providers should stop using the device and follow recall instructions. Manufacturer contact will provide remediation.

Erbe USA
Probes
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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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Health & Personal Care
HIGH
FDA DEVICE

Ion Beam Applications PROTEUS 235 Recalled for 4 Units Worldwide (2026)

Ion Beam Applications S.A. recalled four PROTEUS 235 proton therapy systems distributed worldwide, including Florida in the United States, and the countries of Italy and Japan. The defect disables the Therapy Safety System's Universal Beam Triggering Interface, so the system may not stop beam delivery if the Healthy Signal from an external gating device is lost. Patients and healthcare providers应该

Ion Beam Applications
It was
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Vehicles & Parts
HIGH
NHTSA

Mazda CX-50 Trailer Hitch Recall Affects 2024-2025 SUVs

Mazda North American Operations is recalling certain 2024-2025 CX-50 SUVs equipped with Mazda Genuine Accessory trailer hitches sold through Mazda dealerships. The recall number is 7225C and owner notification letters were mailed April 4, 2025. The recall addresses bolts that may loosen and detach the hitch. Owners should contact their Mazda dealer to schedule a free tightening.

Mazda
A detached
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Tag Statistics

Total Recalls
292

Related Tags

electrical hazardchemical hazardinfant productadult productelderly productimmediate actionstop use immediatelyreturn for refundreplacement availablefda regulatedcpsc regulatednhtsa regulated