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. 1,830 recalls have been distributed to Delaware in the last 12 months.
Showing 20721–20740 of 48,330 recalls
Recalled Item: TRIATHLON FEMORAL DISTAL AUGMENT 10MM - SIZE 2 RIGHT Catalog Recalled by...
The Issue: Due to device overhang issue that protrudes beyond the medial periphery of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LEEP Return Patient Pads (10/ box) Model # 6050Pl used Recalled by...
The Issue: Discrepancy between the correct expiration dates on the individual pouches...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Ketamine 50 mg/5 mL in 0.9% Sodium Chloride Injection for Recalled by SCA...
The Issue: Lack of Assurance of Sterility.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Irrisept Wound Debridement and Cleansing System. 12 units per case. Recalled...
The Issue: Potential defect in the sterile pouch seal, which may result in a lack of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Bioseal Trachea Extender 1/pl 50pk/Cs Recalled by Bioseal Corporation Due to...
The Issue: The reported stress crack in the port of the swivel elbow where the flip cap...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Remisol Advance running on hardware with Windows XP Recalled by Normand-Info...
The Issue: A patch was released for a critical remote code execution vulnerability in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Grab n Go Opti series VIPR system Model # PRX-9646 Recalled by Western /...
The Issue: Limited access to flow settings as a result of the control knob having been...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Grab n Go Opti series VIPR system Model # PRX-9653 Recalled by Western /...
The Issue: Limited access to flow settings as a result of the control knob having been...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Grab n Go Opti series VIPR system Model # PRX-9632 Recalled by Western /...
The Issue: Limited access to flow settings as a result of the control knob having been...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Grab n Go Opti series VIPR system Model # PRX-9627 Recalled by Western /...
The Issue: Limited access to flow settings as a result of the control knob having been...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Grab n Go Opti series VIPR system Model # PRX-9615 Recalled by Western /...
The Issue: Limited access to flow settings as a result of the control knob having been...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atellica IM 1300 Analyzer Recalled by Siemens Healthcare Diagnostics, Inc....
The Issue: Issues Scanning New Reagent Lot Test Definition on the Atellica IM 1300...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atellica IM 1600 Analyzer Recalled by Siemens Healthcare Diagnostics, Inc....
The Issue: Issues Scanning New Reagent Lot Test Definition on the Atellica IM 1300...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RELPAX (eletriptan HBr) tablets Recalled by Pfizer Inc. Due to Microbial...
The Issue: Microbial Contamination of Non-Sterile Products: contamination with...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Aquilex Fluid Control System component: Bag deflector Recalled by WOM World...
The Issue: The deficit displayed by the pump can differ from the real deficit, leading...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atellica IM anti-CCP IgG (aCCP) Assay Siemens Material Number: 10732998...
The Issue: Atellica IM anti-CCP IgG (aCCP) Test Definition (TDef) Mitigation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AssayTip/AssayCup Tray-used on the cobas e 801 module which is Recalled by...
The Issue: AssayTips part of the AssayTip/AssayCup Tray Tips used on the cobas e 801...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EXACTAMED Oral Dispensers Recalled by Baxter Healthcare Corporation Due to...
The Issue: Exactamed 5 mL Oral Dispenser Pharmacy Packs may contain both 5 mL and 3 mL...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: S-GLUTATHIONE 200MG/3ML (PF) INHALATION SOLN Recalled by First Royal Care...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: S-PYRIDOXINE HCL (B6) 100MG/ML MDV Recalled by First Royal Care Co. LLC, dba...
The Issue: Lack of Assurance of Sterility
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.