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. 1,824 recalls have been distributed to Delaware in the last 12 months.
Showing 22061–22080 of 48,330 recalls
Recalled Item: MAHURKAR and Argyle acute hemodialysis catheters Recalled by COVIDIEN LLC...
The Issue: The priming volume values printed on the MAHURKA and Argyle acute catheters...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips IntelliBridge System configured with a regional setting which uses...
The Issue: Infusion Pump Data Storage Accuracy-Data from the BBraun Space LAN or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Patient Information Center iX configured with a regional setting...
The Issue: Infusion Pump Data Storage Accuracy-Data from the BBraun Space LAN or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DEXIS Titanium Intraoral Sensor Product Usage: The DEXIS Titanium Intraoral...
The Issue: The sensor's look up calibration files were incorrectly programmed during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HYDROmorphone 20 mg/100 mL Injectable Solution Recalled by Advanced Pharma...
The Issue: Sub-potency
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Inovo Single Luman Conserver Product Usage: This device is intended Recalled...
The Issue: The pressure gauge (manometer) may dislodge from the threaded...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Aquarius D13S319 Plus Deletion Probe Recalled by Cytocell Ltd. Due to There...
The Issue: There is an error in the chromomap on the package insert.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ThermaCare HEATWRAPS Recalled by PF Consumer Healthcare 1 LLC Due to There...
The Issue: There is the potential that a HeatWrap could include cells that have a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SOLOPATH Balloon Expandable TransFemoral System Recalled by Terumo Medical...
The Issue: There is a potential for dislodgement of the tip from the outer diameter of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Portico Solo Re-Collapsible Access System Recalled by Terumo Medical...
The Issue: There is a potential for dislodgement of the tip from the outer diameter of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SOLOPATH Re-Collapsible Access System Recalled by Terumo Medical Corporation...
The Issue: There is a potential for dislodgement of the tip from the outer diameter of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ThermaCare HEATWRAPS Recalled by PF Consumer Healthcare 1 LLC Due to There...
The Issue: There is the potential that a HeatWrap could include cells that have a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Acyclovir Tablets Recalled by Zydus Pharmaceuticals USA Inc Due to Labeling;...
The Issue: Labeling; Label Mix-up; report received of one bottle labeled as Acyclovir...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Carvedilol Tablets Recalled by Zydus Pharmaceuticals USA Inc Due to...
The Issue: Labeling; Label Mix-up; report received of one bottle labeled as Acyclovir...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Dermoplast Anesthetic PAIN & ITCH (benzocaine and menthol) SPRAY canisters...
The Issue: Labeling: Not Elsewhere Classified: canisters incorrectly state the net...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Dermoplast Anesthetic PAIN & ITCH (benzocaine and menthol) SPRAY canisters...
The Issue: Labeling: Not Elsewhere Classified: Full cases may contain canisters that...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Revonto (dantrolene sodium for injection) Recalled by US Worldmeds LLC Due...
The Issue: Presence of Precipitate: Appearance is Out of Specification for the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Lidar System for Erosion Flume Application Class 1 Laser Product Recalled by...
The Issue: Failure to comply event due to incorrect labeling of a class 1 laser product.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Endoscopic Cleaning Brushes sold in various Endoscopy Kits - Product...
The Issue: Potential risk of brush detachment during cleaning. If brush detachment is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DIVALPROEX SODIUM EXTENDED-RELEASE TABLETS Recalled by MAJOR PHARMACEUTICALS...
The Issue: cGMP deviations: Product was exposed above 50% relative humidity levels...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.