PlainRecalls
FDA Devices Moderate Class II Ongoing

Medichoice Infant Heel Warmer, Reference # 989805643721 1079906

Reported: January 26, 2022 Initiated: November 29, 2021 #Z-0509-2022

Product Description

Medichoice Infant Heel Warmer, Reference # 989805643721 1079906

Reason for Recall

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.

Details

Recalling Firm
Philips North America Llc
Units Affected
2,925,800 units
Distribution
US Nationwide and Canada.
Location
Cambridge, MA

Frequently Asked Questions

What product was recalled?
Medichoice Infant Heel Warmer, Reference # 989805643721 1079906. Recalled by Philips North America Llc. Units affected: 2,925,800 units.
Why was this product recalled?
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.
Which agency issued this recall?
This recall was issued by the FDA Devices on January 26, 2022. Severity: Moderate. Recall number: Z-0509-2022.