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Recall data is sourced from official U.S. government agencies (CPSC, FDA, NHTSA, USDA) and processed using AI to improve readability. This site is not affiliated with or endorsed by any government agency. Always refer to the original agency notice for authoritative information.

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Medium RiskFDA Device

Philips North America Llc: After the device was cleared by the FDA, Philips made changes to the labeling that do not fall within the existing FDA clearance. These devices with the modified labeling cannot be distributed or sold without new 510(k) clearance.; After the device was cleared by the FDA, Philips made changes to the labeling that do not fall within the existing FDA clearance. These devices with the modified labeling cannot be distributed or sold without new 510(k) clearance.

Agency Publication Date: January 19, 2022
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Affected Products

Product: Infant Heel Warmers w/strap, Reference # 989805603201 1223

All units are impacted

Product: Heel Snuggler, Reference # 989805603411 99047

All units are impacted

Product: Cardinal Infant Heel Warmer, Reference # 989805617251 11470-010T

All units are impacted

Product: Medichoice Infant Heel Warmer, Reference # 989805643721 1079906

All units are impacted

Additional Information

Agency: Food and Drug Administration (FDA)
Event ID: 89163
Status: Active
Manufacturer: Philips North America Llc
Manufactured In: United States
Units Affected: 4 products (5,164,600 units; 2,509,100 units (Updated to 2,515,200 as of 2/15/22); 4,920,600 units; 2,925,800 units)

Were You Affected by This Recall?

If you or a family member were harmed by this recalled product, you may have legal rights. Consider consulting a consumer protection attorney to understand your options for compensation.

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AI-Enhanced Content: The summary, action steps, and risk assessment on this page were generated by AI from official government recall data to improve readability. This is not legal or medical advice. Always refer to the official agency sources below for authoritative information.

Sources: FDA iRES · Raw API Response

openFDA Disclaimer: This recall information is sourced from the openFDA API. Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Refer to the openFDA terms of service for more information.