Battery Pack Respironics Model 915 for use in the 900 Series SmartMonitor and the 900 Series Pulse Oximeter.
FDA device recall Z-1220-04 · posted 2004-07-27 · Terminated
Recall details
- Recalling firm
- Respironics, Inc.
- Reason for recall
- Recalling firm received a product complaint from a customer that the lead wire from Model 915 battery was not connected.
- Action taken
- The recalling firm sent a recall letter to their direct accounts, which include parents and vendors regarding the problem associated with the battery packs. The recall letter advised their customers to check their inventory and if the battery pack is one of the affected recalled product to immediately contact their Customer Service Department. to arrange for replacement battery packs.
- Root cause
- Other
- Status
- Terminated
- Product code
- BZQ
- Quantity affected
- 2726 units
- Distribution
- The recalled product was distributed nationwide and internationally to the folllowing states: AL, AR, AZ, CA, CO, CT, FL, GA, IA, ID, IL, IN, KY, LA, MD, ME, MI, MO, MS, MT, NC, ND, NE, NH, NJ, NY, OH
- Date initiated
- 2004-06-04
- Date posted
- 2004-07-27
- Date terminated
- 2005-01-06
- Location
- Murrysville, PA
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