Health & Personal Care
HIGH
FDA DRUG
Zydus Lifesciences Entecavir 1 mg Tablets Recalled for Impurity Degradation Issues (2025)
Zydus Pharmaceuticals USA Inc.
Failed Impurity/Degradation
battery powered Recalls
294 recalls tagged with “battery powered”.
HIGH
CPSC
Makita Recalls 3 Cordless Grease Guns and 4 Hoses Over Laceration Hazard (2025)
Makita U.S.A. recalls 3 cordless grease guns and 4 grease gun hoses due to a laceration hazard. Serial-numbered units are affected. Stop using the recalled equipment immediately and contact Makita for a free replacement hose.
Makita
The flexible
Food & Beverages
HIGH
FDA FOOD
Pacific Coast Producers Pears Sliced in Organic Pear Juice Recall 203 Cases for Lead Contamination (
Potential contamination with heavy metal (Lead).
Pacific Coast Producers
Potential contamination
Health & Personal Care
HIGH
FDA DEVICE
Philips Allura Xper FD20 OR Table Recalled for 174 Units Worldwide in 2025
Philips Medical Systems Nederland
Systems may
Health & Personal Care
HIGH
FDA DEVICE
Philips Medical Systems Nederland B.V. Recalled 98 Imaging Systems for CMOS Battery, HDD, PSU Deteri
Philips Medical Systems Nederland B.V.
Systems may
Health & Personal Care
HIGH
FDA DEVICE
Philips Allura Xper FD10/10 Recall for 286 Units Worldwide in 2025
Philips Medical Systems Nederland B.V.
Systems may
Health & Personal Care
HIGH
FDA DEVICE
Philips Allura Xper FD20/10 Recall 45 Units Worldwide in 2025
Philips Medical Systems Nederland B.V.
Systems may
Health & Personal Care
HIGH
FDA DEVICE
Philips Allura Xper FD20 Biplane Recall Affects 268 Units Worldwide (2025)
Philips Medical Systems
Systems may
Health & Personal Care
HIGH
FDA DEVICE
Philips Allura Xper FD10 Recall 2025: 1,117 Imaging Systems Worldwide Face Movement-Dysfunction Risk
Philips
Systems may
Health & Personal Care
HIGH
FDA DEVICE
Philips Philips Medical Systems Netherlands B.V. Allura Xper FD20/20 OR Table Recall Affects 3 Units
Philips Medical Systems Netherlands B.V.
Systems may
Health & Personal Care
HIGH
FDA DEVICE
Philips Allura Xper FD20/20 Recall Affects 75 Systems Worldwide for Internal Component Deterioration
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
Systems may
Food & Beverages
HIGH
FDA FOOD
New Spirit Naturals Ultra Whey Protein Powder Recalled for Undeclared Milk Allergen
New Spirit Naturals
undeclared allergen
Health & Personal Care
HIGH
FDA DEVICE
Philips Medical Systems Nederland Blames BIOS Battery Design Flaw in Allura Centron 722400 Recall (Z
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
The BIOS
Health & Personal Care
HIGH
FDA DEVICE
Philips Medical Systems Nederland Recall Expands for Allura Xper FD20/15 OR Table Model 722059 (2025
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
The BIOS
Health & Personal Care
HIGH
FDA DEVICE
Philips Medical Systems Nederland recalls 5 Allura Xper FD20/20 OR Tables for BIOS battery startup
Philips Medical Systems Nederland B.V.
The BIOS
Health & Personal Care
HIGH
FDA DEVICE
Philips Medical Systems Nederland Recall: BIOS Battery Causes Startup Failures in Allura Xper CV20 7
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
The BIOS
Health & Personal Care
HIGH
FDA DEVICE
PHILIPS Allura Xper FD10/10 Recall Tied to BIOS Battery Depletion
Philips Medical Systems Nederland B.V.
The BIOS
Health & Personal Care
HIGH
FDA DEVICE
Philips Allura Xper FD20/20 Recall 115 Units Over Startup-Battery Risk (2025)
Philips Medical Systems Nederland
The BIOS
Health & Personal Care
HIGH
FDA DEVICE
Philips Allura Xper FD20 Biplane Recalled for BIOS Battery Failure in 501 Units (2025)
Philips Medical Systems Nederland
The BIOS
Health & Personal Care
HIGH
FDA DEVICE
Philips Allura Xper FD20 BiOS Battery Recall Affects 5,067 Units Worldwide
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
The BIOS