Product Recalls in Maryland
Product recalls affecting Maryland — including food, drugs, consumer products, medical devices, and vehicles distributed to Maryland. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,674 recalls have been distributed to Maryland in the last 12 months.
Showing 25281–25300 of 52,535 recalls
Recalled Item: C2 CryoBalloon Controller Recalled by PENTAX of America Inc Due to The...
The Issue: The Controller does not detect overpressure in the balloon during the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: iTotal CR Total Knee Replacement System Recalled by Conformis, Inc. Due to...
The Issue: The kits were prepared with incorrect patient ID labels and may contain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pentax Medical C2 CryoBalloon Pear Focal Catheter Recalled by PENTAX of...
The Issue: Incorrect default dose and dose increments may be transmitted to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pentax Medical C2 CryoBalloon Standard 90 degree Catheter Recalled by PENTAX...
The Issue: Incorrect default dose and dose increments may be transmitted to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ST AIA-PACK Homocysteine (HCY) is designed for IN VITRO DIAGNOSTIC Recalled...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ST AIA-PACK Testosterone (TES) is designed for IN VITRO DIAGNOSTIC Recalled...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Azurion lnterventional Fluoroscopic X-ray System Recalled by Philips Medical...
The Issue: Philips has discovered through customer complaints and internal testing an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AIA-PACK Folate (FOL) is designed for IN VITRO DIAGNOSTIC USE Recalled by...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ST AIA-PACK ACTH (ACTH: Adrenocorticotropic Hormone) is designed for IN...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BVI Visitec Soft Tip Cannula Recalled by Beaver Visitec Due to Certain lots...
The Issue: Certain lots are missing a protective sheath component over the silicone...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens Biograph Horizon PET/CT System Recalled by Siemens Medical Solutions...
The Issue: Improper design or specifications.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AIA-PACK B12 (Vitamin B12) is designed for IN VITRO DIAGNOSTIC Recalled by...
The Issue: Potential for fluorescein interference to cause inaccurately elevated...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ST AIA-PACK FT3 (FT3: Free Triiodothyronine) is designed for IN Recalled by...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Amlodipine and Olmesartan Medoxomil Tablets Recalled by Aurobindo Pharma USA...
The Issue: Discoloration: This product is being recalled due to a confirmed pharmacist...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: NYSTATIN Oral Suspension Recalled by VistaPharm, Inc. Due to Failed...
The Issue: Failed Impurities/Degradation Specifications:Out of specification for...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: System Recalled by GE Healthcare, LLC Due to GE Healthcare has identified...
The Issue: GE Healthcare has identified that a small number of Nuclear Medicine systems...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: System Recalled by GE Healthcare, LLC Due to GE Healthcare has identified...
The Issue: GE Healthcare has identified that a small number of Nuclear Medicine systems...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vitros Myoglobin Calibrators Recalled by Ortho Clinical Diagnostics Inc Due...
The Issue: A stability issue in the calibrators may cause calibration failures or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tritanium Posterior Lumbar (PL) cage intervertebral body fusion implant....
The Issue: The surgical technique is being updated to caution against misuse due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Maximum Variable Pitch Compression Tray Base Recalled by Zimmer Biomet, Inc....
The Issue: There is a potential for silicone shedding during cleaning and sterilization.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.