infant product Recalls

228 recalls tagged with “infant product”.

Health & Personal Care
HIGH
FDA DEVICE

Philips Respironics Trilogy EV300 Ventilator Recall Affects 113,717 Units in 2026

Philips Respironics recalled 113,717 Trilogy EV300 ventilators sold in the United States and internationally after determining the Obstruction Alarm may fail to trigger within required standards. The alarm can delay alerting caregivers for up to four breaths. Patients and healthcare providers should stop using the device immediately and follow recall instructions from Philips or their clinician.

Philips Respironics
In some
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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
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Food & Beverages
HIGH
FDA FOOD

Savannah Bee Company Honey BBQ Sauce Mustard Recalled for Soy and Wheat Allergens (2026)

4,611 bottles are recalled nationwide. The product is Savannah Bee Company Honey BBQ Sauce Mustard, distributed to numerous states. The bottle actually contains Honey BBQ Sauce 'Sweet' which contains wheat and soy not declared on the Mustard label. Stop using the product and contact Savannah Bee Company for a refund or replacement.

Savannah Bee Company
Undeclared Allergens:
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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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Recalled TheKiddoSpace LED Soccer Hover Ball
HIGH
CPSC

TheKiddoSpace Recalls LED Soccer Hover Balls Over Burn Risk

TheKiddoSpace recalled LED soccer hover balls on February 26, 2026, due to a burn hazard. The balls exceed the allowable surface temperature for batteries, posing serious injury risks. Consumers should stop using these toys immediately and seek a replacement.

TheKiddoSpace
The surface
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Recalled Bicystar High Chair - model TB-HC6900
HIGH
CPSC

Bicystar High Chairs Recalled Due to Fall and Entrapment Risks

Bicystar recalled children's high chairs on February 26, 2026, due to serious fall and entrapment hazards. The affected high chairs lack required crotch restraints, putting children at risk. Consumers should stop using these chairs immediately and seek a refund.

Bicystar High Chairs
The high
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Recalled Babysense Max View 5.5" Baby Monitor display/parent unit
HIGH
CPSC

Babysense Max View Baby Monitors Recalled Due to Fire Hazard

Hisense recalled Babysense Max View baby monitors on February 26 after reports of overheating display units. The recall affects model VBM55, with incidents of sparking during charging. Consumers should stop using the device immediately and contact Hisense for a replacement.

Hisense Ltd., of Israel
The display
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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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Health & Personal Care
HIGH
FDA DEVICE

Siemens Healthcare Diagnostics Atellica CH A1c_E Recall for 21,291 Units (2026)

Siemens Healthcare Diagnostics recalled 21,291 Atellica CH A1c_E units distributed to laboratories nationwide and internationally in 2026. The recall addresses a depressed result bias when A1c_E is processed with RCRP on the same analyzer. Labs using separate analyzers are not impacted. Stop using the affected module immediately and follow manufacturer instructions. Contact Siemens or your lab’s F

Siemens Healthcare Diagnostics
A potential
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Recalled MCS one-piece footed sleepwear - Style 7903815
HIGH
CPSC

Meijer Recalls Children's Sleepwear Due to Burn Hazard

Meijer recalled several styles of children's sleepwear on February 19, 2026, due to a burn hazard. The recall affects various one-piece footed sleepwear for infants sizes 12, 18, and 24 months. Consumers should stop using the sleepwear and return it for a full refund.

Meijer
The recalled
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Food & Beverages
HIGH
FDA FOOD

Sunflour Bakery Recalls 1 Bag Hamburger Bun Over Undeclared Sesame Seed (2026)

Sunflour Bakery recalled 1 bag of Hamburger Bun, 18oz with six buns sold to a single Orange County retailer. The recall involves sesame seeds not declared on the label. Consumers should not eat the product and should contact Sunflour Bakery by email for refund or replacement.

NRS Enterprises, Inc. dba Sunflour Bakery
Undeclared sesame
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Health & Personal Care
HIGH
FDA DEVICE

Mentor Texas CPX 4 US Breast Tissue Expanders Recall 2026

Mentor Texas, LP recalled CPX 4 US Breast Tissue Expanders with Suture Tabs worldwide on February 18, 2026. The recall covers models SCPX-107MH, SCPX-117MH, SCPX-127MH, SCPX-135MH, SCPX-146MH and SCPX-156MH. Infusion sets may include a dull needle tip that is difficult to advance and may break. Stop using the device and follow recall instructions from the manufacturer, with recall notification by-

Mentor Texas
Infusion sets
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Health & Personal Care
HIGH
FDA DEVICE

Mentor CPX 4 Breast Tissue Expanders Recalled in 2026 for Dull Needle Tip Hazard

Mentor Texas LP recalled CPX 4 US Breast Tissue Expanders with Suture Tabs on February 18, 2026. Infusion sets may have dull or blunt needle tips that can be difficult to advance or break. Health facilities and patients should stop using the device immediately and follow the recall instructions.

Mentor Texas LP
Infusion sets
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Health & Personal Care
HIGH
FDA DEVICE

Mentor Texas LP Recalls CPX 4 US Breast Tissue Expanders with Suture Tabs (2026)

Mentor Texas LP recalled CPX 4 US Breast Tissue Expanders with Suture Tabs sold worldwide, including US nationwide, after determining infusion sets may contain a dull needle tip. The defect may hinder needle advancement or cause breakage during use. Patients and providers should stop using the device immediately and follow recall instructions from the manufacturer.

Mentor Texas
Infusion sets
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Tag Statistics

Total Recalls
228

Related Tags

immediate actionreturn for refundfda regulatedcpsc regulatedelectrical hazardholiday productadult productexplosion riskstop use immediatelyreplacement availablebedroomliving room