Food & Beverages
HIGH
FDA FOOD
Gina Marie Bakery Recall: 172 Cases of Vanilla Chocolate Dipped Cookies Recalled for Undeclared Red
Gina Marie Bakery
Undeclared
pet related Recalls
225 recalls tagged with “pet related”.
Health & Personal Care
HIGH
FDA DEVICE
Abbott TactiFlex Sensor Ablation Catheter Recalled for Tip Detachment Risk (2025)
Abbott recalls 399 TactiFlex Sensor Enabled Ablation Catheters after reports of tip detachment during packaging removal. The recall covers devices worldwide. Stop using the device immediately and follow manufacturer instructions.
Abbott
Abbott has
Food & Beverages
HIGH
FDA FOOD
Whole Foods Market Granola Recalled for Undeclared Allergens in 6-Unit Pack
Product was incorrectly labeled, resulting in undeclared wheat, sesame, and cashew.
WFM Purchasing, LP
Product was
Food & Beverages
HIGH
FDA FOOD
Lee K of NY Inc. Recalls 43-Unit Batch of PINOCCHIO CATERING Aged Kimchi Mackerel for Undeclared All
Product contains undeclared milk and shrimp
Lee K of NY
Product contains
Health & Personal Care
HIGH
FDA DEVICE
Philips Ultrasound C9-4 Transducer Recalled for Lifespan Labelling — 1 Unit (2025)
To provide clarification and labelling to define the useful life of ultrasound transducers in the field.
Philips Ultrasound
To provide
Health & Personal Care
HIGH
FDA DEVICE
GE Medical Systems AW Server 2.0, AW Server 3.0, 3.1, 3.2 Recalled For Security Breach Risk (2025)
Firm has identified a security vulnerability in AW Server products. If exploited, a malicious actor could compromise the confidentiality, integrity, and availability of patient data.
GE Medical Systems
Firm has
HIGH
CPSC
URMYWO Baby Loungers Recalled for Suffocation and Fall Hazards; 2025 Recall Active
URMYWO
The baby
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
Food & Beverages
HIGH
FDA FOOD
Gospodarstwo Pasieczne Sadecki Bartnik Bee Pollen 200g Recall for Pyrrolizidine Alkaloids (2025)
Gospodarstwo Pasieczne Sadecki Bartnik
detectable pyrrolizidine
Health & Personal Care
HIGH
FDA DEVICE
American Contract Systems High-Rire Recall: 32,433 Medical Convenience Kits Recalled for Re-GassedEO
American Contract Systems
Identified products
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 DRUG
Zydus Lifesciences Chlorpromazine Hydrochloride 25 mg 100-count Tablets Recalled Nationwide (2025)
CGMP Deviations: presence of N-Nitroso Desmethyl Chlorpromazine above the recommended acceptable intake limit
Chlorpromazine Hydrochloride
CGMP Deviations:
Health & Personal Care
HIGH
FDA DRUG
Sun Pharmaceutical Radiopharmaceutical Kit Recall: 1,870 Kits Recalled for OOS Dissolution Issue
Failed Dissolution Specifications-Out of Specification (OOS) observation for sulphate in Sodium Tartrate Dihydrate used for the production of Mertiatide.
Sun Pharmaceutical Industries
Failed Dissolution
Food & Beverages
HIGH
FDA FOOD
Endico Potatoes Recalls 335 Cases of PEAS & CARROTS for Listeria Contamination (2025)
Product may be contaminated with Listeria monocytogenes.
Endico Potatoes
Product 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 Medical Systems FD20 Biplane OR Table Recall for BIOS Battery Depletion (2025)
PHILIPS MEDICAL SYSTEMS NEDERLAND B.V.
The BIOS
Health & Personal Care
HIGH
FDA DEVICE
Philips Medical Systems Nederland Faces High-Risk Recall for Allura Xper FD20/15 BIOS Battery
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
Inpeco FlexLab X System Potassium Test System Recalled for Unvalidated Hemolysis, Icterus, Lipemia H
Inpeco S.A.
The FlexLab