Battery hazard recalls
Federal recalls citing a battery hazard.
- Past 12 months
- 76
- Past 90 days
- 22
- Past 30 days
- 4
- Past 7 days
- 1
Recall volume — past 12 months
per monthSeverity class
past 12 monthsWhere it shows up
top product categories- Consumer55
- Baby51
- Device21
- Toy14
- Electronics9
- Pet5
- 2025-11-19FDA-DeviceGE HealthcareClass IIPortrait VSM Model nos. 6660000-666 Monitor, Physiological, Patient (With Arrhythmia Detection or Alarms
Potential loss of monitoring on affected monitors when powered by certain batteries. Affected batteries can lose capability to hold charge and provide back up power. If this situation occurs, it will cause loss of patient monitoring and potentially delay recognizing patient status changes requiring treatment.
- 2025-11-19FDA-DeviceGE HealthcareClass IIB105P, B125P, B105M, B125M, B155M Patient Monitors; Model nos. 6160000-002 6160000-003 6160000-004 6160000-005 6160000-101 6160000-102 6160000-103 6160000-104 6160000-105 6160001-063 6160001-064 6160001-065 Monitor, Physiological, Patient (With Arrhythmia Detection or Alarms 3/19/26 updated to add B105P Patient Monitor 6160001-061 B125P Patient Monitor 6160001-062 B105M-C Patient Monitor 6160002-033 B105M-A Patient Monitor 6160000-113 B155M-A Patient Monitor 6160000-115 B125P-B Patient M
Potential loss of monitoring on affected monitors when powered by certain batteries. Affected batteries can lose capability to hold charge and provide back up power. If this situation occurs, it will cause loss of patient monitoring and potentially delay recognizing patient status changes requiring treatment.
- 2025-11-19FDA-DeviceGE HealthcareClass IICARESCAPE ONE, Model no. 2087075-300 - shipped with potentially affected batteries or affected batteries installed as a spare part Monitor, Physiological, Patient (With Arrhythmia Detection or Alarms Updated 3/19 to add CARESCAPE ONE MBZ101 2087075-001
Potential loss of monitoring on affected monitors when powered by certain batteries. Affected batteries can lose capability to hold charge and provide back up power. If this situation occurs, it will cause loss of patient monitoring and potentially delay recognizing patient status changes requiring treatment.
- 2025-11-19FDA-DeviceGE HealthcareClass IICarescape B450, Model no. 5805686 - shipped with potentially affected batteries or affected batteries installed as a spare part Monitor, Physiological, Patient (With Arrhythmia Detection or Alarms Record updated 3/19/26 to include: CARESCAPE B450 MBA313 2095800-001 CARESCAPE MONITOR B450 (ATO MODEL) 2068491-002 CARESCAPE MONITOR B450 B1 2107633-001 CARESCAPE MONITOR B450-GS (V2.0.8) 2094080-001
Potential loss of monitoring on affected monitors when powered by certain batteries. Affected batteries can lose capability to hold charge and provide back up power. If this situation occurs, it will cause loss of patient monitoring and potentially delay recognizing patient status changes requiring treatment.
- 2025-11-13CPSCGreat Lakes CheeseGreat Lakes Wholesale International Recalls Select Battery Packs Due to Battery Ingestion; Violates Federal Statute for Child-Resistant Packaging of Button Cell and Coin Batteries
The button cell and lithium coin batteries are not in child-resistant packaging and do not bear the warning labels required under Reese's Law. If a child swallows button cell or coin batteries, the ingested batteries can cause serious injuries, including internal chemical burns and death.
- 2025-11-13CPSCXingziguBettina Doll Sets Recalled Due to Risk of Serious Injury or Death from Battery Ingestion; Violates Mandatory Standard for Toys; Sold on Amazon by Shantou Chenghai Xingzigu Toy Industry
The doll sets violate the mandatory standard for toys because the battery compartment of the unicorn contains button cell batteries that can be easily accessed by children. When button cell or coin batteries are swallowed, the ingested batteries can cause serious injuries, internal chemical burns and death.
- 2025-11-12FDA-DeviceB-K MedicalClass IIbk5000 Ultrasound System w/battery; Model No. 2300-61; System, Imaging, Pulsed Doppler, Ultrasonic
GE HealthCare has become aware that the Instructions for Use within the user guide and service manual do not adequately state the required battery replacement intervals, end-of-life handling procedures, or general battery safety precautions.
- 2025-11-12FDA-DeviceB-K MedicalClass IIbk3500 Ultrasound System w/battery; Model No. 2300-41; System, Imaging, Pulsed Doppler, Ultrasonic
GE HealthCare has become aware that the Instructions for Use within the user guide and service manual do not adequately state the required battery replacement intervals, end-of-life handling procedures, or general battery safety precautions.
- 2025-11-12FDA-DeviceB-K MedicalClass IIbk3000 Ultrasound System w/battery; Model No. 2300-66; System, Imaging, Pulsed Doppler, Ultrasonic
GE HealthCare has become aware that the Instructions for Use within the user guide and service manual do not adequately state the required battery replacement intervals, end-of-life handling procedures, or general battery safety precautions.
- 2025-11-12FDA-DeviceB-K MedicalClass IIUUltrasound System 2300, bkActiv w/battery; Model No. 2300-11; System, Imaging, Pulsed Doppler, Ultrasonic
GE HealthCare has become aware that the Instructions for Use within the user guide and service manual do not adequately state the required battery replacement intervals, end-of-life handling procedures, or general battery safety precautions.
- 2025-11-12FDA-DeviceB-K MedicalClass IIUltrasound System 1300, bkSpecto w/battery; Model No. 1300-21 or 1300-S1; System, Imaging, Pulsed Doppler, Ultrasonic
GE HealthCare has become aware that the Instructions for Use within the user guide and service manual do not adequately state the required battery replacement intervals, end-of-life handling procedures, or general battery safety precautions.
- 2025-11-12FDA-DeviceB-K MedicalClass II1202 Flex Focus Ultrasound System, cart models UA1214 and UA1814, used with: Flex Focus 200, Flex Focus 300, Flex Focus 400, Flex Focus 500, Flex Focus 700, Flex Focus 800; System, Imaging, Pulsed Doppler, Ultrasonic
GE HealthCare has become aware that the Instructions for Use within the user guide and service manual do not adequately state the required battery replacement intervals, end-of-life handling procedures, or general battery safety precautions.
- 2025-11-06CPSCSefon StoreNapei Infant Bath Tubs Recalled Due to Risk of Serious Injury or Death from Ingestion Hazard; Violates Mandatory Standard for Consumer Products with Button Cell Batteries; Sold on Amazon by Sefon Store
The recalled infant bath tubs violate the mandatory standard for consumer products containing button cell or coin batteries because the built-in thermometer contains button cell batteries that can be accessed easily by children. When button cell or coin batteries are swallowed, the ingested batteries can cause serious injuries, internal chemical burns and death.
- 2025-10-09CPSCBmrwtgBmrwtg LED tutu skirts recalled for coin battery ingestion risk
Bmrwtg LED tutu skirts sold on Amazon contain lithium coin batteries that children can easily access and swallow. When swallowed, these batteries can cause serious internal burns and death. The skirts also lack required safety warnings.
- 2025-10-08FDA-DevicePhilipsClass IICheck your Philips Allura Xper FD10 system
Certain Philips Allura Xper FD10 X-ray systems may have a BIOS battery that depletes faster than expected, preventing the system from starting up. The system will not display any warning before the battery runs out of power.
- 2025-10-08FDA-DevicePhilipsClass IIContact Philips about Allura Xper FD10C system failure
The BIOS battery in some Philips Allura Xper FD10C X-ray systems may run out of power faster than expected. When this happens, the system will not start up, and there are no warning messages to alert users before the battery fails.
Get notified about new battery hazard recalls
Free weekly digest. We email when new federal recalls are published — including this hazard.
Get the Sunday Brief