Pfizer Recalls PureSilk Shave Gel for Women Due to Rupture Risk
Pfizer is recalling PureSilk Shave Gel for women because the can liner may corrode and rupture, potentially propelling sharp components.
What this means for you
Real risk of harm even if no illness or injury has been reported yet. Stop using the product and follow the agency's guidance.
Our severity reasoning: The recall involves a risk-of-harm product where the can may rupture and propel sharp components, but the source explicitly states that no injuries have been reported, fitting the High severity criteria for unreported injury risks.
Plain-English summary
Pfizer is voluntarily recalling cans of PureSilk Shave Gel for women sold between October 1995 and June 1996. The recall is being conducted in cooperation with the U.S. Consumer Product Safety Commission (CPSC). The inner liner of the cans may corrode, causing the can to rupture. This rupture could propel a plastic component or the gel from the can, posing a risk of injury from sharp edges or the plastic parts.
More than 500,000 purple, seven-ounce cans were sold nationwide at drug, grocery, and cosmetic stores for between $2 and $2.50. Pfizer is aware of 10 incidents of the cans rupturing, but no injuries have been reported. This recall does not affect the PureSilk Shave Cream product.
Consumers should stop using the shave gel immediately and discharge the gel to reduce pressure within the can. They should record the lot number printed on the bottom of the container and then discard the can. To receive a free replacement certificate or a refund, consumers should send their name, address, and the container lot number to Pfizer Consumer Health Care - Consumer Relations Dept., 235 East 42nd Street, New York, N.Y. 10017-5755, or call (800) 723-7529 for more information.
The recalled product
- Product
- PureSilk Shave Gel for women
- Manufacturer
- Pfizer
- Category
- Consumer Product — Personal Care
- Hazard
Distribution
Distributed nationwide across the United States.
Related recalls
Same manufacturer · Pfizer
See all →- HighLevoxyl 50 microgram levothyroxine tablets recalled as a subpotent drug
FDA (Drugs) · 2025-08-20
- SevereDrug recall: Bleomycin injection vials recalled due to glass contamination
FDA (Drugs) · 2024-01-31
- SeverePfizer Recalls Daptomycin Injection Due to Microbial Contamination
FDA (Drugs) · 2018-08-08
Same hazard · laceration
See all →- Severe
- High
- HighOBP Medical Recalls Vaginal Speculums Due to Potential Sharp Edges
FDA (Devices) · 2026-08-19
- SevereDR Power PRO MAX30 Lawn Mowers Recalled Over Blade Control Hazard
CPSC · 2026-08-06
- Severe