HIGH
CPSC
Vive Health Bed Rails Recall Expands as Entrapment, Asphyxiation Risk Causes Two Deaths
Vive Health
When the
infant product Recalls
794 recalls tagged with “infant product”.
Food & Beverages
HIGH
FDA FOOD
Connecticut Crab Company Crab Cakes Recalled for Temperature Abuse Risk, 39 Boxes Affected
May be temperature abused, which may result in growth of Clostridium botulinum
Connecticut Crab Company
May be
Health & Personal Care
HIGH
FDA DRUG
Omnipaque Injection Recalled by GE Healthcare for Particulate Matter in 866,570 vials (2026)
OMNIPAQUE
Presence of
Health & Personal Care
HIGH
FDA DRUG
GE Healthcare Omnipaque Iohexol Injection Recall Expanded for Particulate Matter in 306,810 Vials (D
OMNIPAQUE
Presence of
Health & Personal Care
HIGH
FDA DRUG
Fagron Compounding Services Vancomycin HCI Recall: 34,260 Bags with Break-Off-Part Risk (2026)
Lack of Assurance of Sterility; blue Break-Off-Part could detach from the administration port
Fagron Compounding Services
Lack of
Health & Personal Care
HIGH
FDA DRUG
Fagron Compounding Services Vancomycin HCl 1 g in 250 mL NS Injection Recall Expands in 2026
Lack of Assurance of Sterility; blue Break-Off-Part could detach from the administration port
Fagron Compounding Services
Lack of
Health & Personal Care
HIGH
FDA DRUG
Fagron Compounding Services Norepinephrine Bitartrate Injection Recall Affects 5,140 Bags (2026)
Lack of Assurance of Sterility; blue Break-Off-Part could detach from the administration port
Fagron Compounding Services
Lack of
Health & Personal Care
HIGH
FDA DRUG
Clonidine Transdermal System Recall Expanded for CGMP Deviations in 113,943 Cartons (2026)
Teva-affiliated Clonidine Transdermal System recalls 113,943 cartons after CGMP deviations. Unapproved raw material prompts recall. Stop use immediately and contact Teva or a healthcare provider for guidance.
CLONIDINE TRANSDERMAL SYSTEM
CGMP Deviations:
HIGH
CPSC
Wagner Spray Tech Recalls 900-Series Power Steamers Over Burn Hazard (2026)
Wagner Spray Tech
The attached
HIGH
HIGH
CPSC
Electrolux Group Recalls Frigidaire Gas Ranges for Burn Hazard (2026)
Electrolux Consumer Products, Inc., of Charlotte, North Carolina
The ovens
MEDIUM
CPSC
Tainoki Fine Furniture Recalls 3 Office Chairs Over Fall Hazard (2026)
Tainoki Fine Furniture
The recalled
HIGH
CPSC
Lifetime Brands Recalls BUILT LUUM Light Up Tumblers for Choking and Battery Ingestion Hazards (2026
Lifetime Brands
The recalled
Health & Personal Care
HIGH
FDA DRUG
Teva Octreotide Acetate Injectable Suspension Recall 21,930 Cartons Over Sterility Risk (2026)
Lack of Assurance of Sterility: Quality system deficiencies identified during a routine U.S Food and Drug Administration (FDA) inspection at the contract manufacturer.
OCTREOTIDE ACETATE
Lack of
Health & Personal Care
HIGH
FDA DRUG
Curosurf 240 mg Poractant Alfa Recalled for Sterility Concerns (2026)
Chiesi USA recalled 7,235 Curosurf vials distributed nationwide to hospitals and clinics. The recall cites a lack of assurance of sterility. Healthcare providers should stop using the product immediately and contact Chiesi USA for guidance.
CUROSURF
Lack of
Health & Personal Care
HIGH
FDA DRUG
Teva Octreotide Acetate Injectable Suspension Recall 19,869 Cartons Nationwide (2026)
Lack of Assurance of Sterility: Quality system deficiencies identified during a routine U.S Food and Drug Administration (FDA) inspection at the contract manufacturer.
OCTREOTIDE ACETATE
Lack of
Health & Personal Care
HIGH
FDA DRUG
Xanax XR Alprazolam Recall Over Failed Dissolution Specifications Affects US Nationwide Distribution
XANAX
Failed Dissolution
Health & Personal Care
HIGH
FDA DRUG
Cipla USA Lanreotide Injection Recall for Sterility Assurance Issue (2026)
Lack of Assurance of Sterility: Due to an FDA observation at the contract manufacturing site for deficiencies in their visual inspection procedure.
LANREOTIDE ACETATE
Lack of
Food & Beverages
HIGH
FDA FOOD
Pure Vitamins and Natural Supplements Blue Bull Extreme Recall for undeclared sildenafil (High risk)
FDA analysis revealed the presence of undeclared sildenafil
Pure Vitamins and Natural Supplements
FDA analysis
Health & Personal Care
HIGH
FDA DRUG
Lanreotide Injection recall: Cipla USA lanreotide acetate pre-filled syringes recalled for sterility
Lack of Assurance of Sterility: Due to an FDA observation at the contract manufacturing site for deficiencies in their visual inspection procedure.
LANREOTIDE ACETATE
Lack of