Philips Medical Systems HeartStart Pads Pediatric Plus, Pediatric Plus Multifunction Defibrillation Electrode Pads Model M3717A Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
HeartStart Pads Pediatric Plus, Pediatric Plus Multifunction Defibrillation Electrode Pads Model M3717A
Brand
Philips Medical Systems
Lot Codes / Batch Numbers
Lot Number : Y042005-1
Products Sold
Lot Number : Y042005-1
Philips Medical Systems is recalling HeartStart Pads Pediatric Plus, Pediatric Plus Multifunction Defibrillation Electrode Pads Model M due to The Apex/Anterior and the Sternum/Posterior pad labels are located in reverse position to the wire and connector. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
The Apex/Anterior and the Sternum/Posterior pad labels are located in reverse position to the wire and connector
Recommended Action
Per FDA guidance
Philips Medical sent the recall notification letter 11/30/05 via FedEx
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