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. 997 recalls have been distributed to Delaware in the last 12 months.
Showing 18321–18340 of 48,330 recalls
Recalled Item: Accurian RF Ablation Recalled by Medtronic Sofamor Danek USA Inc Due to...
The Issue: Insertion difficulty of the probes. The probe was catching on a lip inside...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Accurian RF Ablation Recalled by Medtronic Sofamor Danek USA Inc Due to...
The Issue: Insertion difficulty of the probes. The probe was catching on a lip inside...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Accurian RF Ablation Recalled by Medtronic Sofamor Danek USA Inc Due to...
The Issue: Insertion difficulty of the probes. The probe was catching on a lip inside...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 1.8mm Truss Wire Recalled by New Standard Device Inc Due to 1.8mm truss...
The Issue: 1.8mm truss wires are being removed to facilitate the introduction of 2.0mm...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA Chemistry Calibrator Recalled by Siemens Healthcare Diagnostics, Inc....
The Issue: Calibration errors have been observed with the Total and Direct Bilirubin...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: STAT KIT Z-1000 emergency medical kit HealthFirst - Product Usage: Recalled...
The Issue: A missing component (hand suction pump) in the emergency medical kits.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GlideScope Core OneTouch Smart Cable Recalled by Verathon, Inc. Due to When...
The Issue: When video laryngoscopy system users apply, twisting motions while...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Tube Set for TEM - Product Usage: Transanal Endoscopic Microsurgery Recalled...
The Issue: Tube material of a smaller diameter was used.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atellica CH Chemistry Calibrator Recalled by Siemens Healthcare Diagnostics,...
The Issue: Calibration errors have been observed with the Total and Direct Bilirubin...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OrthoPediatrics ACL Reconstruction System ShieldLoc 7mm implant component...
The Issue: ShieldLoc implant component of the ACL Reconstruction Systemlots may be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OrthoPediatrics ACL Reconstruction System ShieldLoc 6mm implant component...
The Issue: ShieldLoc implant component of the ACL Reconstruction Systemlots may be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: StealthStation" S7 System with Polaris Spectra Camera part number PSU...
The Issue: There is a potential for specific camera units to be affected by a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Time-Cap Labs Recalled by Marksans Pharma Limited Due to CGMP Deviations:...
The Issue: CGMP Deviations: FDA analysis detected N-Nitrosodimethylamine (NDMA)...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Prednisolone Sodium Phosphate Oral Solution Recalled by Akorn, Inc. Due to...
The Issue: Discoloration: Out of Specification (OOS) result for APHA Color Test.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Brimonidine Tartrate Opthalmic Solution 0.2% Recalled by SOMERSET...
The Issue: Failed Impurities/Degradation Specification: There is a slow leaching...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Metformin Hydrochloride Extended-Release Tablets Recalled by AVKARE Inc. Due...
The Issue: CGMP Deviations: FDA analysis detected N-Nitrosodimethylamine (NDMA)...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Metformin Hydrochloride Extended-Release Tablets Recalled by AVKARE Inc. Due...
The Issue: CGMP Deviations: FDA analysis detected N-Nitrosodimethylamine (NDMA)...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Brimonidine Tartrate Opthalmic Solution 0.2% Recalled by SOMERSET...
The Issue: Failed Impurities/Degradation Specification: There is a slow leaching...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Brimonidine Tartrate Opthalmic Solution 0.2% Recalled by SOMERSET...
The Issue: Failed Impurities/Degradation Specification: There is a slow leaching...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Ablation Galil Technology Recalled by Boston Scientific Corporation Due to...
The Issue: The needle surface deteriorated due to unexpected electrolysis during procedure.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.