FDA recall record

Pintler Medical A warming pad, a component of the PINTLER PEAK & PINTLER SUMMIT Heated OR recall — FDA Z-1139-2019

Malfunction warming pad.

Class IIclassification
Z-1139-2019official record ID
Apr 24, 2019report date

Recall record at a glance

Official recordZ-1139-2019
CategoryMedical Device Recalls
ClassificationClass II
FDA record statusCompleted
Recalling firmPintler Medical LLC
Report dateApr 24, 2019
Recall initiation dateApr 20, 2018
Quantity24
LocationPhilipsburg, MT, United States

Official product description

A warming pad, a component of the PINTLER PEAK & PINTLER SUMMIT Heated OR pad. PPWS-001 indicated for use in any condition where patient warming is desired as determined by clinical personnel, in accordance with facility normo-thermia protocol

Why the product was recalled

Malfunction warming pad.

Distribution information

US Distribution to state of: Wisconsin.

How to read the classification

FDA Class II indicates a situation in which use of or exposure to the product may cause temporary or medically reversible adverse health consequences, or where the probability of serious consequences is remote. The classification shown here comes from the FDA record.

Additional record details

Recall type: Voluntary: Firm initiated. Initial notification: Visit.

What to do next

If you believe you have the recalled product, use the recall number and firm information above to confirm the official notice and follow the instructions issued by the FDA, recalling firm, retailer or product manufacturer. For drugs and medical devices, decisions about treatment or medical care should be discussed with a qualified health professional.

About this record

Recall Lookup USA preserves the most complete source information successfully retrieved. We do not create missing facts or infer affected lots or VINs. The official record may still change, so use the identifier above when verifying current instructions.

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