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. 2,582 recalls have been distributed to Delaware in the last 12 months.
Showing 15021–15040 of 27,373 recalls
Recalled Item: RAPIDPoint 405 Blood Gas Analyzer Recalled by Siemens Healthcare...
The Issue: Therapeutic levels (1mg/mL and 2mg/mL) of Hydroxocobalamin may interfere...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AlIura Xper F010 F Recalled by Philips Electronics North America Corporation...
The Issue: There is a potential for the Monitor Ceiling Suspension, which holds a large...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Poly C- DMCP-Visub(H3000) Recalled by Philips Electronics North America...
The Issue: There is a potential for the Monitor Ceiling Suspension, which holds a large...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Allura Xper F020 Biplane DR Table Recalled by Philips Electronics North...
The Issue: There is a potential for the Monitor Ceiling Suspension, which holds a large...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Allura Xper F020 DR Table Recalled by Philips Electronics North America...
The Issue: There is a potential for the Monitor Ceiling Suspension, which holds a large...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AIIuraXperFDlO Recalled by Philips Electronics North America Corporation Due...
The Issue: There is a potential for the Monitor Ceiling Suspension, which holds a large...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: INTEGRIS SUITE Recalled by Philips Electronics North America Corporation Due...
The Issue: There is a potential for the Monitor Ceiling Suspension, which holds a large...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AIIura Xper F010 DR Table Recalled by Philips Electronics North America...
The Issue: There is a potential for the Monitor Ceiling Suspension, which holds a large...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Allura Xper FD2O Recalled by Philips Electronics North America Corporation...
The Issue: There is a potential for the Monitor Ceiling Suspension, which holds a large...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: INTEGRIS Allura 9 (biplane) Recalled by Philips Electronics North America...
The Issue: There is a potential for the Monitor Ceiling Suspension, which holds a large...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CoLink(TM) Lapidus Plate XP Recalled by In2bones USA, LLC Due to CoLink(TM)...
The Issue: CoLink(TM) Lapidus Plate +2mm Right and Left, were laser marked incorrectly....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Allura Xper FD2O Biplane Recalled by Philips Electronics North America...
The Issue: There is a potential for the Monitor Ceiling Suspension, which holds a large...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Allura Xper FD2O Recalled by Philips Electronics North America Corporation...
The Issue: There is a potential for the Monitor Ceiling Suspension, which holds a large...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Haemonetics OrthoPAT System-Integrated Set. Product Code: 1150H-00 OrthoPAT...
The Issue: OrthoPAT¿ reservoirs are missing the cannula inside the reservoirs. The...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 2008T HEMODIALYSIS SYSTEM W/BIBAG Recalled by Fresenius Medical Care Renal...
The Issue: In the hemodialysis machine during the cleaning/disinfection program, when...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips SureSigns VS4 Vital Signs Monitor Recalled by Philips Electronics...
The Issue: Philips has received several reports in which monitors with lithium ion...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips SureSigns VS2 monitor Recalled by Philips Electronics North America...
The Issue: Philips has received several reports in which monitors with lithium ion...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Portex Pulsator Arterial Blood Sampling Kit with Dry Lithium Heparin...
The Issue: The product was mislabeled with the incorrect label.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips SureSigns VM 3/4/6/8 Patient Monitors Recalled by Philips...
The Issue: Philips has received several reports in which monitors with lithium ion...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Haemonetics¿ OrthoPAT¿ System-OPAT QuickConnect Reservoirs. Product Code:...
The Issue: OrthoPAT¿ reservoirs are missing the cannula inside the reservoirs. The...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.