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. 2,572 recalls have been distributed to Delaware in the last 12 months.
Showing 17261–17280 of 27,373 recalls
Recalled Item: Single-Lumen Central Venous Catheterization Kit with Blue FlexTip(R)...
The Issue: Arrow International is recalling the affected product because the packaging...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Multi-Lumen Central Venous Catheterization Kit with Blue FlexTip(R) Recalled...
The Issue: Arrow International is recalling the affected product because the packaging...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 1) Pressure Injectable Multi-Lumen Central Venous Catheterization Kit 2)...
The Issue: Arrow International is recalling the affected product because the packaging...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 1) Pressure Injectable ARROW(R) PICC Kit with Chlorag+ard(R) Technology The...
The Issue: Arrow International is recalling the affected product because the packaging...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arrow Pressure Injectable PICC Kit Catheter Recalled by Arrow International...
The Issue: The Arrow Pressure Injectable PICC is intended for short-term or long-term...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 1) Introducer Kit with Integral Hemostasis Valve/Side Port Recalled by Arrow...
The Issue: Arrow International is recalling the affected product because the packaging...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arterial Catheterization Kit Recalled by Arrow International Inc Due to...
The Issue: Arrow International is recalling the affected product because the packaging...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ARROWg+ard Blue CVC Kit The ARROWg+ard Blue CVCs are intended Recalled by...
The Issue: The Arrow CVC is indicated to provide short-term (<30 days) central venous...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Covidien Endo Peanut 5mm Auto Suture Blunt Dissector Item Code: Recalled by...
The Issue: Cotton tip of the device may disengage due to insufficient adhesive
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arrow Multi-Lumen CVC Kit The Arrow Two-Lumen Central Venous Access Recalled...
The Issue: The Arrow CVC is indicated to provide short-term (<30 days) central venous...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arrow MAC Two-Lumen Central Venous Access Kit Introducer Catheter The...
The Issue: Arrow International is recalling the affected product because the packaging...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Merge PACS software. The firm name on the label is Merge Healthcare Recalled...
The Issue: Merge PACS did not show unviewed images when the last view was skipped....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Merge PACS software. Merge PACS (Picture Archiving Communication System) is...
The Issue: When cut lines are shown on an image, the lines may go from being vertical...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Reusable instruments in the Knee Recalled by Zimmer Biomet, Inc. Due to...
The Issue: Durability characteristics of reusable instruments were not established
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Her2/Neu (c-erbB-2) (CB-1 1) Recalled by Cell Marque Corporation Due to Cell...
The Issue: Cell Marque has determined the need to issue a product recall after...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Estrogen Receptor (SP1) 7.0 mL Catalog number 249R-18 Recalled by Cell...
The Issue: Cell Marque has determined the need to issue a product recall after...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SV40 (MRQ-4) 0.5 ml catalog number 351 M-15. Microbiology - Recalled by Cell...
The Issue: Cell Marque has determined the need to issue a product recall after...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Estrogen Receptor (EP1) 7.0 mL Catalog number 249R-28 Recalled by Cell...
The Issue: Cell Marque has determined the need to issue a product recall after...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CD117 Recalled by Cell Marque Corporation Due to Cell Marque has determined...
The Issue: Cell Marque has determined the need to issue a product recall after...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: H. pylori (polyclonal} 1.0 mL Catalog number 215A-76 Recalled by Cell Marque...
The Issue: Cell Marque has determined the need to issue a product recall after...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.