Drug recall

Thermacare HEATWRAPS JOINT PAIN THERAPY, 8 HEATWRAPS; MUSCLE PAIN THERAPY, 3 HEATWRAPS a) UPC 0573301311 b)…

FDA recall event 81178 · Class II · Pfizer Inc.

Key facts

Event ID 81178
Recall numbers Z-0554-2019, Z-0555-2019, Z-0556-2019
Recalling firm Pfizer Inc.
Product type Devices
Products 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…, Thermacare HeatWraps Menstrual a) UPC 0573302002 b) UPC 0573302044 Product Usage: Provides heat therapy for temporary relief of minor menstrual cramp pain and associated back aches., Thermacare Muscle Pain Therapy HeatWraps: a) UPC 0573301314 b) UPC 0573301303 Product Usage: Provides heat therapy for temporary relief of minor muscular and joint aches and pains associated with…
Classification Class II
Status Terminated
Voluntary or mandated Firm Initiated
Reason for recall The firm received complaints of the wrap coming apart and leaking granular material
Initiation date Oct 2, 2018
Report date Dec 12, 2018
Termination date Aug 28, 2023
City New York
State NY
Country United States
FEI number 2416101

At a glance

  • 1–9 Products in this recall
  • 10–99 FDA inspections of this firm (FEI)

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

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