toddler product Recalls

292 recalls tagged with “toddler product”.

Health & Personal Care
HIGH
FDA DEVICE

Cook Medical Recall: Cook Staged Extubation Set Labeled with Expired Dates in 2026 Class II Recall

Cook Medical issued a global recall of 95 units of the Cook Staged Extubation Set due to expiration dates that exceed true shelf life. The affected lots carry Reference Part Number C-CAE-14.0-83-EXTU and Order Number G24073. The recall is classified as HIGH hazard. Patients and healthcare providers should stop using the device immediately and follow recall instructions from Cook Incorporated.

Cook
Products from
Read more
Health & Personal Care
HIGH
FDA DEVICE

Philips Azurion 7 M20 X-ray System Recall Affects 5,167 Units Worldwide (2026)

Philips Medical Systems Nederland recalled 5,167 Azurion 7 M20 X-ray imaging systems sold to healthcare facilities in the U.S. and internationally. The wired foot switch can fail to initiate imaging or produce intermittent imaging. Hospitals and clinics should stop using the device and follow recall instructions from Philips, with notification by letter to affected parties.

Philips Medical Systems Nederland
Philips has
Read more
Health & Personal Care
HIGH
FDA DEVICE

Philips Allura Xper FD20/10 Recall Affects 85 Imaging Systems in 2026

Philips recalled 85 Allura Xper FD20/10 imaging systems distributed nationwide and internationally. The devices may fail to initiate X-ray imaging or do so intermittently when using the wired foot switch. Hospitals and clinicians should stop using the device and follow the manufacturer’s recall instructions.

PHILIPS MEDICAL SYSTEMS NEDERLAND
Philips has
Read more
Health & Personal Care
CRITICAL
FDA DEVICE

Philips Respironics Trilogy Evo O2 Ventilator Recall Affects 113,717 Units in 2026

Philips Respironics recalls 113,717 Trilogy Evo O2 home-use ventilators in 2026. The Obstruction Alarm may fail to trigger within required standards, delaying warning for airway obstruction for up to four breaths. Stop using the device and follow recall instructions from Philips or your clinician.

Philips Respironics
In some
Read more
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,
Read more
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
Read more
Health & Personal Care
HIGH
FDA DEVICE

Medline NAMIC Angiographic Syringe Recall Affects 17,902 Kits Worldwide (2026)

Medline Industries, LP recalls 17,902 medical convenience kits worldwide after post-market surveillance found a potential risk of the syringe rotating adaptor unwinding. The recall covers NAMIC Angiographic RA control syringes labeled in 10 Medline SKUs. Healthcare providers should stop use immediately and follow recall instructions.

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

Medline NAMIC Angiographic Rotating Adaptor Syringe Recall Affects 762 Units Worldwide (2026)

Medline Industries, LP recalls 762 medical convenience kits containing NAMIC Angiographic Rotating Adaptor syringes sold worldwide, including the U.S., PR, Canada, and several international markets. The recall cites a potential risk that the syringe rotating adaptor may unwind during use, creating a loose connection or disconnect between the syringe and the manifold. Stop using the device and seek

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

Medline NAMIC RA Syringe Adaptor Recall Aims to Prevent Connection Failures in 60 Kits (2026)

Medline Industries, LP recalled 60 medical convenience kits worldwide due to a potential rotating adaptor unwinding in NAMIC Angiographic RA control syringes. The issue may cause a loose connection or disconnection between the syringe and manifold. Healthcare providers should stop using the device and follow the manufacturer’s recall instructions.

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

Medline NAMIC Angiographic RA Syringes Recalled in 1698 Kits for Unwinding Adaptor Risk (2026)

Medline Industries, LP recalls 1,698 medical convenience kits worldwide over a potential unwind of the NAMIC Angiographic Rotating Adaptor during use. The risk could cause a loose connection or complete disconnection between the syringe and manifold. Healthcare providers and patients should stop using the affected kits immediately and follow recall instructions.

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

Medline NAMIC RA Syringe Recall: 108 Units Worldwide for Unwinding Adaptor (High Risk)

Medline Industries, LP recalls 108 NAMIC Angiographic Rotating Adaptor Syringes sold worldwide, including the United States, PR and several international markets. The rotating adaptor may unwind during use, creating a loose connection or disconnection with the manifold. Healthcare providers must stop using the device and follow recall instructions.

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

Medline NAMIC Angiographic Syringe Recall for 2,154 Kits Worldwide

Medline Industries, LP recalls 2,154 medical convenience kits worldwide after post-market surveillance found a risk that the NAMIC Angiographic Rotating Adaptor may unwind. A loose connection or disconnection between the syringe and manifold could occur. Stop using immediately and follow manufacturer recall instructions.

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

Medline NAMIC Angiographic Rotating Adaptor Syringes Recalled in 82 Kits Worldwide

Medline Industries, LP recalled 82 medical convenience kits containing NAMIC Angiographic Rotating Adaptor syringes. The recall covers two Medline SKUs and spans worldwide distribution, including the US, Puerto Rico and several countries. The defect is a rotating adaptor that may unwind, causing loose connections or disconnections between syringe and manifold.

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

Medline NAMIC Angiographic Syringe Recall for 1.75 Million Kits Over Adaptor Unwinding Risk (2026)

Medline Industries, LP recalls 1,752,096 NAMIC Angiographic Syringe kits worldwide, including the US and Canada. The recall stems from a post-market signal about the rotating adaptor unwinding during use. This may cause a loose connection or disconnection between the syringe and manifold. Health care providers and patients should stop using the devices and follow recall instructions.

Medline Industries, LP
Medline Industries,
Read more
Previous
12345...15
Next

Tag Statistics

Total Recalls
292

Related Tags

chemical hazardexplosion riskelectrical hazardsuffocation riskinfant productchildren productadult productelderly productfederal law violationcpsc regulatedreplacement availablestop use immediately