Empty D aluminum oxygen cylinders packaged in shipping containers labeled as: Product #0022-44P, CYL 02 ALUM 400 LITER,
FDA device recall Z-2032-2009 · posted 2009-09-10 · Terminated
Recall details
- Recalling firm
- Allied Healthcare Products Inc
- Reason for recall
- Medical valves do not meet quality specifications which may cause the valve to fail and result in uncontrolled release of oxygen when the valve is in the open position.
- Action taken
- The recalling firm first notified their customers via a letter dated 5/15/09 issued regular mail explaining the reason for recall and requesting the cylinders with specific post valves be returned. A second letter dated 6/1/09 was issued via regular mail which provided specific shipping dates that each customer received the suspect product. Neither of these two letters requested subrecall. A third letter dated 6/17/09, which included copies of the first two letters, via certified mail. This letter informed the customer the recall was to be conducted to the user level and requested their customer conduct a subrecall. Requested to remove the cylinder from service and call Allied Healthcare Products for return and a replacement at 1-800-268-1661.
- Root cause
- Nonconforming Material/Component
- Status
- Terminated
- Product code
- ECX
- Quantity affected
- 32 cylinders
- Distribution
- Class II Recall Worldwide Distribution including states of NY, NC, KY, PA, WI, NH, NJ, CA, CT, FL and Singapore.
- Date initiated
- 2009-05-15
- Date posted
- 2009-09-10
- Date terminated
- 2012-04-23
- Location
- St. Louis, MO
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