infant product Recalls

794 recalls tagged with “infant product”.

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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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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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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Food & Beverages
HIGH
FDA FOOD

Made Fresh Salads Strawberry Cream Cheese 5 lb Tub Recalled for Listeria Contamination (2026)

Made Fresh Salads recalled 557 five-pound tubs of Strawberry Cream Cheese after a Listeria monocytogenes contamination was identified. The recall covers all expiration dates through 2/27/2026 and distribution is limited to New York. Consumers should not consume the product and should contact Made Fresh Salads Inc by telephone for refund or replacement.

Made Fresh Salads
Products may
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Food & Beverages
HIGH
FDA FOOD

Made Fresh Salads Garlic & Herb Cream Cheese 5 lb Tub Recalled for Listeria Contamination (2026)

Made Fresh Salads Inc recalled 557 five-pound tubs of Garlic & Herb Cream Cheese sold in New York after a confirmed Listeria monocytogenes contamination. The recall was activated on February 19, 2026 and remains active as of March 18, 2026. Consumers who purchased the product should not consume it and should contact the company for refund or replacement guidance.

Made Fresh Salads
Products may
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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 Artoura Breast Tissue Expanders Recall for Dull Needle Tips (2026)

Mentor Texas, LP is recalling Artoura Breast Tissue Expanders with infusion sets worldwide, including the United States and Canada. The infusion sets may contain dull or blunt needle tips that are difficult to advance or may break. Patients and healthcare providers should stop using the device and follow recall instructions.

Mentor
Infusion sets
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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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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 DRUG

Kirkman MAXIMUM Zone 1 4% Lidocaine Cream Recall 178 Bottles (2026)

Kirkman recalled 178 bottles of MAXIMUM Zone 1 4% Lidocaine Cream distributed nationwide in the U.S. by Dermal Source. The recall cites stability data that does not support the stated expiry date. Consumers and healthcare providers should stop using this product immediately and contact Kirkman for guidance.

Kirkman
Stability Data
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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

Abiomed Impella Automated Controller Recall 62 Units in 2026

Abiomed recalled 62 Automated Impella Controller units sold to hospitals internationally. The recall warns of a delayed Purge System Blocked alarm display when used with first generation Impella 5.5 pumps. Hospitals should stop using the device immediately and contact Abiomed for instructions.

Abiomed
Potential that
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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 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

Medtronic MiniMed 530G Insulin Pumps Recalled for Delivery Errors in 2026 (13,429 Units)

Medtronic recalled 13,429 MiniMed insulin pumps worldwide after identifying unintended insulin delivery errors. The issue occurs when the pump height relative to the infusion site changes, causing over-delivery or under-delivery of insulin. Patients should stop using the device and contact Medtronic for instructions.

Medtronic MiniMed
All Medtronic
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Tag Statistics

Total Recalls
794

Related Tags

laceration riskimmediate actionstop use immediatelyreturn for refundelectrical hazardsuffocation risktip over riskfire hazardbattery poweredtoddler productchildren productadult product