Infa-Therm Transport Mattress, Reference Number 989805616831 1015 — FDA record Z-0505-2022

Reported ongoing

Status as reported in the agency record. FDA warns that enforcement status may not track the current recall lifecycle; check the current official notice.

Source date Nov 26, 2021. Retrieved Oct 1, 2026. Last updated Oct 1, 2026.

Archive changed Oct 1, 2026. USDA FSIS records are unavailable; check FSIS directly. Source coverage and dates.

What the record says

Product
Infa-Therm Transport Mattress, Reference Number 989805616831 1015
Reason
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.
Classification
Class II
Recalling firm
Philips North America Llc
Quantity
141,744 units (Updated to 141,750 units as of 2/15/22)
Agency-reported status
Ongoing
Source record identifier
Z-0505-2022

Open the official record

What the recall classes mean. Classification is an agency assessment, not individual medical advice.

Lot and product identifiers

Label fieldDetails supplied by the agency
Lot, code or applicabilityAll units are impacted

Match all identifying details in the current notice. A brand name alone is not enough.

Distribution

US Nationwide and Canada

States below are derived from the distribution text, including nationwide wording. They are not inferred from the firm's address.

Dates in the source

Report date
Jan 26, 2022
Recall initiation date
Nov 26, 2021
Center classification date
Jan 18, 2022

FDA company pages use the listing date; enforcement records use initiation dates; CPSC uses recall date; NHTSA uses report-received date. These dates are not interchangeable.

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