Triad lubricating jelly products, distributed by Triad from Jan. 2007-Dec. 2010, have been recalled due to potential sterilization problems, according to an FDA news release.
Patients who are immuno-compromised, such as those with diabetes, cancer and certain other chronic diseases, may be at risk for infection.
Product may be contained in kits, packs or trays that have been packaged after Dec. 2010 by other firms, including brand names Allegiance, Select Medical Products, Novaplus, Triad, Triad Plus, IMCO, McKesson Medi-Pak Performance and Henry Schein.
Read the news release about the Triad sterile lubricating jelly recall.
Read other coverage about FDA recalls:
- Anesthesiology Devices Recalled After Weak Oversight by FDA
- Study: Recalled Medical Devices Were Cleared Through Less-Stringent 510(k) Process
- Cumberland Pharmaceuticals to Recall Six Lots of Acetadote
Patients who are immuno-compromised, such as those with diabetes, cancer and certain other chronic diseases, may be at risk for infection.
Product may be contained in kits, packs or trays that have been packaged after Dec. 2010 by other firms, including brand names Allegiance, Select Medical Products, Novaplus, Triad, Triad Plus, IMCO, McKesson Medi-Pak Performance and Henry Schein.
Read the news release about the Triad sterile lubricating jelly recall.
Read other coverage about FDA recalls:
- Anesthesiology Devices Recalled After Weak Oversight by FDA
- Study: Recalled Medical Devices Were Cleared Through Less-Stringent 510(k) Process
- Cumberland Pharmaceuticals to Recall Six Lots of Acetadote
