Integra Pain Management Radiation Reduction Gloves, sterile, Latex-free, Catalog No. SSR1-7.0, SSR1-7.5, SSR1-8.0, Integra Pain Management, 3395 West 1820 South, Salt Lake City, Utah 84104. Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Radiation Reduction Gloves, sterile, Latex-free, Catalog No. SSR1-7.0, SSR1-7.5, SSR1-8.0, Integra Pain Management, 3395 West 1820 South, Salt Lake City, Utah 84104.
Brand
Integra Pain Management
Lot Codes / Batch Numbers
Lot No: W0806178, W0806179, and W0806177
Products Sold
Lot No: W0806178, W0806179, and W0806177
Integra Pain Management is recalling Radiation Reduction Gloves, sterile, Latex-free, Catalog No. SSR1-7.0, SSR1-7.5, SSR1-8.0, Integra P due to Radiation reduction gloves were labeled as "Latex-free", but contain natural rubber latex.. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Radiation reduction gloves were labeled as "Latex-free", but contain natural rubber latex.
Recommended Action
Per FDA guidance
On 07/03/2008, all consignees were notified by telephone and letter titled URGENT MEDICAL DEVICE RECALL. They were instructed to immediately cease distribution/use of any affected product and arrange for its return. Contact number for Integra is 800-241-2210.
Verify this information on the official source
For complete details and official instructions, check the U.S. Food and Drug Administration (FDA) directly.
View official FDA recall noticeDistribution
As reported by FDA
AL, CA, FL, LA, NY, OR, SC, TX
Page updated: Jan 10, 2026