Philips North America LLC Philips, HEARTSTART, INFANT/CHILD - SMART PADS CARTRIDGE, REF: M5072A, (0-8 YEARS)< 55 lbs / 25 kg, CE 0123, NON-STERILE, Rx only, UDI: (01) 00884838023758 for use with defibrillator Recall
Check Your Product
According to the U.S. Food and Drug Administration (FDA)
Product
Philips, HEARTSTART, INFANT/CHILD - SMART PADS CARTRIDGE, REF: M5072A, (0-8 YEARS)< 55 lbs / 25 kg, CE 0123, NON-STERILE, Rx only, UDI: (01) 00884838023758 for use with defibrillator
Brand
Philips North America LLC
Lot Codes / Batch Numbers
Lot Y111220-01
Products Sold
Lot Y111220-01
Philips North America LLC is recalling Philips, HEARTSTART, INFANT/CHILD - SMART PADS CARTRIDGE, REF: M5072A, (0-8 YEARS)< 55 lbs / 25 kg, due to Infant/Child defibrillator pads contain incorrect labeling. This could lead to a delay in therapy, or delivery of lower energy than indicated for an a. Based on FDA medical device recall database.
Summary derived from FDA notice
Reason for Recall
As stated by FDA
Infant/Child defibrillator pads contain incorrect labeling. This could lead to a delay in therapy, or delivery of lower energy than indicated for an adult patient
Recommended Action
Per FDA guidance
On July 26, 2021, Phillips issued an "Urgent Medical Device Removal" notification to affected consignees. On August 23, 2021, Phillips issued a revised "Urgent Medical Device Removal notification to update their recall strategy concerning replacement infant/child smart pads cartridges. In addition to informing consignees about the recalled product, Phillips asked consignees to take the following actions: Action 1: If needed, contact your distributor to request a replacement. Customers who purchased their pads cartridges directly from Philips will receive their replacements without any further action on their part. Customers who purchases their pads cartridges from a distributor should contact that distributor to request replacement. Replacement pads cartridges may not be available immediately, therefore, refer to Action 2, below. Action 2: Determine if the Infant/Child SMART Pads may remain in service until replaced. 1. Philips, or your Philips Distributor, will supply a replacement of all M5072A Infant/Child SMART Pads Cartridges from Lot Number Y111220-01. 2. If the Infant/Child SMART Pads Cartridge is still inside the pouch, then it can remain in service until replaced. While waiting to receive the replacement, customers should keep the Infant/Child SMART Pads Cartridge inside the outer pouch until the cartridge is replaced, or until it is needed for therapy. The reason is because the pouch correctly identifies the cartridge as intended for infant/child patients. (Figure 7). 3. If the Infant/Child SMART Pads Cartridge has been removed from the outer pouch, and if the protective cover shows a drawing of pads placement for a child s chest and back, then it can remain in service until replaced. The reason is because the protective cover has the correct image with the image of a child s chest and back. (Figure 8). 4. If the Infant/Child SMART Pads Cartridge has been removed from the outer pouch, and if the protective cover shows a dra
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