Health & Personal Care
HIGH
FDA DEVICE
Summa Therapeutics Recalls 22 Finesse BTK Multicath Angioplasty Balloons Over Burst Specifications (
Potential for the balloon in the device to not meet burst specifications.
Finesse BTK Multicath
Potential for
Drug Recalls Center
2,090 pharmaceutical and medication recalls tracked. Stay informed about FDA drug safety alerts, prescription medications, over-the-counter drugs, and dietary supplements.
2,090
Total Drug Recalls
24
High Risk Medications
FDA
Official Source
Important Medication Safety Information
- Do not stop taking prescribed medications without consulting your healthcare provider
- Contact your pharmacist or doctor if you have a recalled medication
- Check lot numbers carefully - not all batches may be affected
- Return recalled medications to your pharmacy for proper disposal
Looking for a specific drug? Use the search page to find recalls by medication name, manufacturer, or NDC number.
Health & Personal Care
HIGH
FDA DEVICE
DJO Surgical ALTIVATE Glenoid Reamer Head Recall Expands to 927 Units
Their is a potential that the reamer may kick or bind up during or immediately prior to use.
DJO Surgical
Their is
Health & Personal Care
HIGH
FDA DEVICE
DJO Surgical ALTIVATE Reversed Wedge Glenoid Reamer Boss Drill 6.5mm Recalled in 2025 for Binding or
Their is a potential that the reamer may kick or bind up during or immediately prior to use.
DJO Surgical
Their is
Health & Personal Care
HIGH
FDA DEVICE
DJO Surgical Recalls 447 ALTIVATE Reverse Glenoid Reamer Sleeve Units (2025)
Their is a potential that the reamer may kick or bind up during or immediately prior to use.
DJO Surgical
Their is
Health & Personal Care
HIGH
FDA DEVICE
DJO Surgical AltiVate Reverse Glenoid Tray Recall Affects 439 Kits Nationwide (2025)
DJO Surgical recall affects 439 AltiVate Reverse Glenoid Tray kits distributed across 26 states and Puerto Rico. A reamer in the kit may kick or bind during use. Patients and clinicians should stop using the device and follow manufacturer instructions.
DJO Surgical
Their is
Health & Personal Care
HIGH
FDA DEVICE
C.R. Bard Recall: SureStep Foley Tray System Lubri-Sil I.C. Complete Care Contains Incorrect Inserts
C.R. Bard
Foley catheter
Health & Personal Care
HIGH
FDA DRUG
DermaSarra External Analgesic Recalled for Burkholderia Cepecia Contamination (DermaRite Industries)
Microbial Contamination of Non-Sterile Drug Product: The products were found to be contaminated with the bacteria Burkholderia cepecia.
DERMASARRA
Microbial Contamination
Health & Personal Care
HIGH
FDA DEVICE
Quest International Measles IgM 01-190M Recall for False Premarket Clearance
Measles IgM Test Kit lacks premarket approval or clearance.
Quest International
Measles IgM
Health & Personal Care
HIGH
FDA DRUG
DermaKleen Antiseptic Lotion Soap Recalled Nationwide for Burkholderia cepacia Contamination (Class
Microbial Contamination of Non-Sterile Drug Product: The products were found to be contaminated with the bacteria Burkholderia cepecia.
DERMAKLEEN
Microbial Contamination
Health & Personal Care
HIGH
FDA DEVICE
CR Bard Recalls SureStep Foley Tray System A942216 for Incorrect Inserts (2025)
CR Bard
Foley catheter
Health & Personal Care
HIGH
FDA DRUG
PeriGiene Health Care Antiseptic Recalled for Burkholderia Contamination (2025)
Microbial Contamination of Non-Sterile Drug Product: The products were found to be contaminated with the bacteria Burkholderia cepecia.
PeriGiene
Microbial Contamination
Health & Personal Care
HIGH
FDA DRUG
6,973 KleenFoam Antimicrobial Foam Soap Cartridges Recalled for Contamination Risk
Microbial Contamination of Non-Sterile Drug Product: The products were found to be contaminated with the bacteria Burkholderia cepecia.
KleenFoam
Microbial Contamination
Health & Personal Care
HIGH
FDA DEVICE
C.R. Bard Recalls 4,300 SureStep Foley Tray System Bardex I.C. Complete Care Catheter Trays (A303316
C.R. Bard
Foley catheter
Health & Personal Care
HIGH
FDA DEVICE
Stryker Communications Recalls 40 Medical Light Systems Over Powder Coating Chip Risk (2025)
Surgical lights have stress lines forming on the powder coating, which indicates that powder coating chipping can occur.
Stryker Communications
Surgical lights
Health & Personal Care
HIGH
FDA DEVICE
BioFire Defense FilmArray NGDS Warrior Panel NGDS-ASY-0007 Recall 130 Kits in 2025
FilmArray NGDS Warrior Panel (NGDS-ASY-0007) has an increased risk of internal control failures when testing positive blood culture, which may lead to delayed results and additional diagnostic workup.
BioFire Defense
FilmArray NGDS
Health & Personal Care
HIGH
FDA DRUG
Boothwyn Pharmacy Semaglutide Injection Recall for Subpotent Drug (High-Risk)
Boothwyn Pharmacy
Subpotent Drug
Health & Personal Care
HIGH
FDA DRUG
Boothwyn Pharmacy Fluorescein 2% Ophth 3 mL Recall for Subpotent Drug (High Risk)
Boothwyn Pharmacy recalls 8 vials of Fluorescein 2% Ophth 3 mL nationwide after a subpotent drug finding. The recall was issued July 9, 2025 and remains active.
Boothwyn Pharmacy
Subpotent Drug
Health & Personal Care
HIGH
FDA DRUG
Boothwyn Pharmacy Semaglutide Injection Recall for Subpotent Drug (4 mL, 2.5 mg/mL)
Boothwyn Pharmacy
Subpotent Drug
Health & Personal Care
HIGH
FDA DRUG
Boothwyn Pharmacy Semaglutide 2.5 mg/mL 2 mL Vials Recalled for Subpotent Drug (HIGH)
Boothwyn Pharmacy
Subpotent Drug
Health & Personal Care
HIGH
FDA DEVICE
Boston Scientific Neuromodulation Recall Affects 25,260 Vercise DBS Systems Over Wire Break Risk
Boston Scientific Neuromodulation
Wire break(s)
Health & Personal Care
HIGH
FDA DRUG
66,000 Good Neighbor Pharmacy Alcohol Prep Pads Recalled for Subpotent Isopropyl Alcohol Levels
Subpotent Drug- isopropyl alcohol levels fall below the labeled concentration.
Good Neighbor Pharmacy
Subpotent Drug-
Health & Personal Care
HIGH
FDA DRUG
Walmart ReliOn Sterile Alcohol Swabs Recalled for Subpotent Isopropyl Alcohol (2025)
Subpotent Drug- isopropyl alcohol levels fall below the labeled concentration.
Walmart
Subpotent Drug-
Health & Personal Care
HIGH
FDA DRUG
CURAD Alcohol Prep Pads Recall for Subpotent Isopropyl Alcohol (2025)
Subpotent Drug- isopropyl alcohol levels fall below the labeled concentration.
CURAD
Subpotent Drug-
Health & Personal Care
HIGH
FDA DRUG
Medline Alcohol Prep Pads Recalled for Subpotent Isopropyl Alcohol in 6669874 Units
Subpotent Drug- isopropyl alcohol levels fall below the labeled concentration.
Medline Alcohol Prep
Subpotent Drug-
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