Sunrise Medical DeVilbiss PD1000A Pulse Dose Oxygen Conserving Cylinder Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
DeVilbiss PD1000A Pulse Dose Oxygen Conserving Cylinder
Brand
Sunrise Medical
Lot Codes / Batch Numbers
Model PD1000A-M4, serial numbers 06AM4111006 through 06AM4111055, Model PD1000A-M6, serial numbers 06AM6111008 through 06AM6114328, Model PD1000A-ML6, serial numbers 06AML111006 through 06AML111922, Model PD1000A-C, serial numbers 06AC0111001 through 06AC0111191, Model PD1000A-D, serial numbers 06AD0111011 through 06AD0111132, and Model PD1000A-E, serial numbers 06AE0111006-06AE0111267.
Products Sold
Model PD1000A-M4, serial numbers 06AM4111006 through 06AM4111055; Model PD1000A-M6, serial numbers 06AM6111008 through 06AM6114328; Model PD1000A-ML6, serial numbers 06AML111006 through 06AML111922; Model PD1000A-C, serial numbers 06AC0111001 through 06AC0111191; Model PD1000A-D, serial numbers 06AD0111011 through 06AD0111132; and Model PD1000A-E, serial numbers 06AE0111006-06AE0111267.
Sunrise Medical is recalling DeVilbiss PD1000A Pulse Dose Oxygen Conserving Cylinder due to Cylinder could lose oxygen at high pressure after the filling process. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Cylinder could lose oxygen at high pressure after the filling process
Recommended Action
Per FDA guidance
The recalling firm began to notify customer via telephone on 1/24/07. An ''Urgent Medical Device Recall Letter'' was sent on 1/29/07. Customers were advised what model and serial numbers were affected and how to contact the firm and/or dealer to have the unit replaced. The recalling firm identified additional serial numbers that were involved in the recall therefore another Urgent Medical Device Recall Letter dated 6/12/07 was sent to the customers that received the addiitonal units.
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