FDA Device recall Z-0556-2019
Thermacare HEATWRAPS JOINT PAIN THERAPY, 8 HEATWRAPS
- FDA Device
- Class II
- terminated
- Published 2018-12-12
On 2018-12-12 the FDA classified a Class II recall of Thermacare HEATWRAPS JOINT PAIN THERAPY, 8 HEATWRAPS by Pfizer, citing the firm received complaints of the wrap coming apart and leaking granular material.
Read the official FDA Device notice
| Agency | FDA Device |
|---|---|
| Recall number | Z-0556-2019 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2018-10-02 |
| Published | 2018-12-12 |
| Last updated | 2026-09-13 11:54 UTC |
| Company | Pfizer |
| Distribution | US |
Product
Thermacare HEATWRAPS JOINT PAIN THERAPY, 8 HEATWRAPS; MUSCLE PAIN THERAPY, 3 HEATWRAPS a) UPC 0573301311 b) UPC 0573301311 Product Usage: Provides heat therapy for temporary relief of minor muscular and joint aches and pains associated with overexertion, sprains, and arthritis.
Reason
The firm received complaints of the wrap coming apart and leaking granular material
Identifiers
| code_info | a) UPC 0573301311 Bundled Lot Number 8054HA Carton/Pouch Number T26686 b) UPC 0573301311 Bundled Lot Number 8054HB Carton/Pouch Number T26686 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:54 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/device/enforcement.json?search=recall_number:%22Z-0556-2019%22
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