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. 2,825 recalls have been distributed to Maryland in the last 12 months.
Showing 12001–12020 of 29,093 recalls
Recalled Item: BD PosiFlush SF Saline Flush Syringe 10 mL used in Recalled by Access...
The Issue: Saline Flush Syringe compromised sterility due to holes in the packaging.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD PosiFlush SF Saline Flush Syringe 10 mL used in Recalled by Access...
The Issue: Saline Flush Syringe compromised sterility due to holes in the packaging.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD PosiFlush SF Saline Flush Syringe 10 mL used in Recalled by Access...
The Issue: Saline Flush Syringe compromised sterility due to holes in the packaging.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD PosiFlush SF Saline Flush Syringe 10 mL used in Recalled by Access...
The Issue: Saline Flush Syringe compromised sterility due to holes in the packaging.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD PosiFlush SF Saline Flush Syringe 10 mL used in Recalled by Access...
The Issue: Saline Flush Syringe compromised sterility due to holes in the packaging.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD PosiFlush SF Saline Flush Syringe 10 mL used in Recalled by Access...
The Issue: Saline Flush Syringe compromised sterility due to holes in the packaging.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD PosiFlush SF Saline Flush Syringe 10 mL used in Recalled by Access...
The Issue: Saline Flush Syringe compromised sterility due to holes in the packaging.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD PosiFlush SF Saline Flush Syringe 10 mL used in Recalled by Access...
The Issue: Saline Flush Syringe compromised sterility due to holes in the packaging.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD PosiFlush SF Saline Flush Syringe 10 mL used in Recalled by Access...
The Issue: Saline Flush Syringe compromised sterility due to holes in the packaging.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD PosiFlush SF Saline Flush Syringe 10 mL used in Recalled by Access...
The Issue: Saline Flush Syringe compromised sterility due to holes in the packaging.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pump Tube Set for MMS Libra and Solar Systems - Recalled by LABORIE MEDICAL...
The Issue: This field correction is being initiated to address potentially damaged...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PENTARAY NAV HIGH-DENSITY MAPPING CATHETER ELECTRODE EA 22 Rx only Recalled...
The Issue: Mapping Catheter can become entrapped in the cardiac valvular apparatus...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PENTARAY NAV eco HIGH-DENSITY MAPPING CATHETER ELECTRODE EA 22 Rx Recalled...
The Issue: Mapping Catheter can become entrapped in the cardiac valvular apparatus...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARTIS Pheno - Interventional Fluoroscopic X-Ray System Model: 10849000 -...
The Issue: If the C-arm leaves its intended travel path due to a fault within the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BioPlex 2200 Syphilis Total & RPR Linked Immunoabsorption Assay Recalled by...
The Issue: The increased level of RPR reactivity in the BioPlex 2200 Syphilis Total &...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Proteus 235 The Proton Therapy System - Proteus 235 (brand Recalled by Ion...
The Issue: Signature from the user is necessary to proceed with specific actions in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips HeartStart XL Monitor/Defibrillators Model number: M4735A - Product...
The Issue: HeartStart XL MonitorlDefibrillators may not have been included in prior...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Oscar 2 Recalled by Suntech Medical, Inc. Due to The device display, when...
The Issue: The device display, when activated, can show an incorrect decimal point when...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Regard. Item number: 830034. GS0348D- CVC Triple Lumen 20CM non Sulfa-Mercy....
The Issue: Custom procedure kits contains affected lots of PosiFlush Syringe, a product...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TRUE METRIX SELF MONITORING BLOOD GLUCOSE SYSTEM - Product Usage: Recalled...
The Issue: One (1) TRUE METRIX AIR blood glucose meter distributed in the United States...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.