Product Recalls in Delaware
Product recalls affecting Delaware — including food, drugs, consumer products, medical devices, and vehicles distributed to Delaware. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 1,069 recalls have been distributed to Delaware in the last 12 months.
Showing 9941–9960 of 27,373 recalls
Recalled Item: Prodisc C - prosthesis Recalled by Centinel Spine, Inc. Due to Centinel...
The Issue: Centinel Spine learned through five customer complaints that the product was...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA 2120i (RoHS) with Single Aspirate Autosampler (SMN 11219529) - OUS...
The Issue: Potential Sample Identification (SID) Mismatch with14-Character Barcodes
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA 2120i Dual Aspirate (SMN 11314045) - US Recalled by Siemens Healthcare...
The Issue: Potential Sample Identification (SID) Mismatch with14-Character Barcodes
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA 2120i Dual Aspirate (SMN 11314045) - OUS Recalled by Siemens...
The Issue: Potential Sample Identification (SID) Mismatch with14-Character Barcodes
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA 2120i (RoHS) Dual Aspirate Autosampler (SMN 11219530) - OUS Recalled...
The Issue: Potential Sample Identification (SID) Mismatch with14-Character Barcodes
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MAMBA Flex 135 Microcatheter. Packaged with protective sleeve over catheter...
The Issue: The firm initiated a removal of certain batches of MAMBA 135 and MAMBA Flex...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MAMBA Microcatheter. Packaged with protective sleeve over catheter Recalled...
The Issue: The firm initiated a removal of certain batches of MAMBA 135 and MAMBA Flex...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA 2120i (RoHS) with Single Aspirate Autosampler (SMN 11219529) - US...
The Issue: Potential Sample Identification (SID) Mismatch with14-Character Barcodes
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA 2120i Dual Aspirate Autosampler (SMN 10285573) - US Recalled by...
The Issue: Potential Sample Identification (SID) Mismatch with14-Character Barcodes
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA 2120 SAA AUTOSAMPLER (SMN 10374453) - US Recalled by Siemens...
The Issue: Potential Sample Identification (SID) Mismatch with14-Character Barcodes
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA 2120i Single Aspirate (SMN 11314044) - US Recalled by Siemens...
The Issue: Potential Sample Identification (SID) Mismatch with14-Character Barcodes
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA 2120i with Single Aspirate Autosampler (SMN 10488923) - US Recalled by...
The Issue: Potential Sample Identification (SID) Mismatch with14-Character Barcodes
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Covidien Signia Small Diameter Curved Tip Intelligent Reload 45 mm Recalled...
The Issue: Potential for the device safety interlock to fail. The safety interlock...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Regard Recalled by ROi CPS LLC Due to ROi CPS, LLC has become aware, through...
The Issue: ROi CPS, LLC has become aware, through a vendor issued urgent medical device...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Covidien Signia Grey Small Diameter Curved Tip Intelligent Reload 30...
The Issue: Potential for the device safety interlock to fail. The safety interlock...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Covidien Signia Small Diameter Curved Tip Intelligent Reload 30 mm Recalled...
The Issue: Potential for the device safety interlock to fail. The safety interlock...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sensis/ Sensis Vibe Hemo systems with VD12A software as follows: Recalled by...
The Issue: Due to the configuration of certain Windows Service Permissions within the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Software versions syngo.CT VA30A_SP2 or syngo.CT VA30A_SP2a in the Computed...
The Issue: SOMATOM systems-issues in with software syngo.CT VA30A_SP2 or syngo.CT...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Alaris Infusion Pump Module Model 8100 Pump Module Keypad Recalled by...
The Issue: Pump Module keypad lifting, and Fluid ingress could result in 1)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RayCare 3B (3.1.0.60341) - Product Usage: Intended Use Oncology information...
The Issue: Patient related messages created in RayCare 3B, RayCare 4A will be lost when...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.