Recall Z-0556-2019— Pfizer Inc.
Class II · Terminated
Class II FDA medical device recall by Pfizer Inc., initiated 2018-10-02, terminated 2023-08-28. FDA's recall record names no specific 510(k) clearance for this event. 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.
- Recalling firm
- Pfizer Inc.
- Classification
- Class II
- Status
- Terminated
- Initiated
- 2018-10-02
- Terminated
- 2023-08-28
- Firm location
- New York, NY, United States
Product description
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 for recall
The firm received complaints of the wrap coming apart and leaking granular material
Data sourced from openFDA. This site is unofficial and independent of the FDA.