Battery Pack Respironics Model 915 for use in the 900 Series SmartMonitor and the 900 Series Pulse Oximeter.
This recall has been terminated (originally issued July 27, 2004).
- Company
- Respironics, Inc.
- Recall Initiated
- June 4, 2004
- Posted
- July 27, 2004
- Terminated
- January 6, 2005
- Recall Number
- Z-1220-04
- Quantity
- 2726 units
- Firm Location
- Murrysville, PA
- Official Source
- View on FDA website ↗
Reason for Recall
Recalling firm received a product complaint from a customer that the lead wire from Model 915 battery was not connected.
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, OK, OR, PA, RI, SC, SD, TN, TX, UT, VA, WI, WV . In regards to foreign accounts, the product was distributed to Canada and British Columbia.
Lot / Code Info
Model Number 915 Manufacturing Lot Number 45-03
Root Cause
Other
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.