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. 2,668 recalls have been distributed to Delaware in the last 12 months.
Showing 5861–5880 of 48,330 recalls
Recalled Item: Tirzepatide 10 mg/0.5 mL Sterile Solution Recalled by Revive Rx LLC dba...
The Issue: Labeling: Label Mix-up - product labeled as tirzepatide contains...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Amphotericin B Liposome for Injection Recalled by SUN PHARMACEUTICAL...
The Issue: Out of specification for assay
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: GloStrips Recalled by Nomax Inc Due to Failed Impurities/Degradation...
The Issue: Failed Impurities/Degradation Specifications: The Active Pharmaceutical...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: FUL-GLO Recalled by Nomax Inc Due to Failed Impurities/Degradation...
The Issue: Failed Impurities/Degradation Specifications: The Active Pharmaceutical...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: GloStrips Recalled by Nomax Inc Due to Failed Impurities/Degradation...
The Issue: Failed Impurities/Degradation Specifications: The Active Pharmaceutical...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: FUL-GLO Recalled by Nomax Inc Due to Failed Impurities/Degradation...
The Issue: Failed Impurities/Degradation Specifications: The Active Pharmaceutical...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Patient Information Center iX and Patient Information Center iX Expand...
The Issue: Event Catalog information does not save when copied and transferred from one...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Synchro2 Guidewires are a steerable guidewire family with a Recalled by...
The Issue: Stryker Neurovascular has observed an increased frequency of PTFE coating...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alaris Pump Infusion Set Low Sorbing Tubing (PE Lined) Back Recalled by BD...
The Issue: Due to infusion set tubing drip chamber becoming detached from the tubing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Synchro SELECT Guidewires are a steerable guidewire family with Recalled...
The Issue: Stryker Neurovascular has observed an increased frequency of PTFE coating...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The Synchro Neuro Guidewires are a steerable guidewire family with Recalled...
The Issue: Stryker Neurovascular has observed an increased frequency of PTFE coating...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OES 4000 Hysteroscope Recalled by Olympus Corporation of the Americas Due to...
The Issue: The required leakage test was not performed following of a re-work for a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vercise Genus Deep Brain Stimulation (DBS) Implantable Pulse Generator IPG:...
The Issue: Deep Brain Stimulation (DBS) Implantable Pulse Generator (IPG) may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Optum Nimbus II Plus Recalled by OptumHealth Care Solutions LLC Due to...
The Issue: Nimbus II Plus, Infusion Pump Systems, manufactured by InfuTronix, are being...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Pain Wizard Recalled by ARG Laboratories, Inc. Due to Out of Specification...
The Issue: Out of Specification for active ingredient. Violative grade of propylene...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Pain Wizard Recalled by ARG Laboratories, Inc. Due to Out of Specification...
The Issue: Out of Specification for active ingredient. Violative grade of propylene...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: NATURAL PAIN RELIEVING CREAM Recalled by ARG Laboratories, Inc. Due to Out...
The Issue: Out of Specification for active ingredient. Violative grade of propylene...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: NATURAL PAIN RELIEVING CREAM Recalled by ARG Laboratories, Inc. Due to Out...
The Issue: Out of Specification for active ingredient. Violative grade of propylene...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: NATURAL PAIN RELIEVING CREAM Recalled by ARG Laboratories, Inc. Due to Out...
The Issue: Out of Specification for active ingredient. Violative grade of propylene...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: NATURAL PAIN RELIEVING CREAM Recalled by ARG Laboratories, Inc. Due to Out...
The Issue: Out of Specification for active ingredient. Violative grade of propylene...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.