Intermed Gas Products Corporation Post Medical Valves VO870A-Y and VO870-A-Y-T PSI 2015, PSI 2015, CGA 870, Inlet .750 STDS, Gas services (Oxygen), PSI 2015, Aluminum Cylinders, InterMed Gas Products LLC Industrial Division, 2056 Vista Parkway West Palm Beach, FL 33411. Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Post Medical Valves VO870A-Y and VO870-A-Y-T PSI 2015, PSI 2015, CGA 870, Inlet .750 STDS, Gas services (Oxygen), PSI 2015, Aluminum Cylinders, InterMed Gas Products LLC Industrial Division, 2056 Vista Parkway West Palm Beach, FL 33411.
Brand
Intermed Gas Products Corporation
Lot Codes / Batch Numbers
Batch Numbers: 08-05-3B and 09-01-1B.
Products Sold
Batch Numbers: 08-05-3B and 09-01-1B.
Intermed Gas Products Corporation is recalling Post Medical Valves VO870A-Y and VO870-A-Y-T PSI 2015, PSI 2015, CGA 870, Inlet .750 STDS, Gas ser due to Firm received reports from customers that valves malfunctioned when installation and/or filling process. Customers forwarded pictures of the defect wh. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Firm received reports from customers that valves malfunctioned when installation and/or filling process. Customers forwarded pictures of the defect where the top portion of the packing nut broke off from the threaded portion of the net; which may cause the valve to fail and result in uncontrolled release of oxygen when the valve is in the open position.
Recommended Action
Per FDA guidance
Intermed Gas Products Corporation notified customers of the affected product by phone beginning March 27, 2009 and followed up with a formal "Product Recall Notice" letter dated March 31, 2009. All affected product should be located and returned to the firm for replacement. For further information, contact Intermed Gas Products at 1-561-483-1364.
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 noticePage updated: Jan 10, 2026