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. 2,495 recalls have been distributed to Delaware in the last 12 months.
Showing 21041–21060 of 27,373 recalls
Recalled Item: OmniPod¿ Insulin Management System. Only the OmniPod¿ device is affected....
The Issue: OmniPods¿ (Pods) have a higher rate of failure causing: Cannula fails to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OmniPod¿ Insulin Management System. Only the OmniPod¿ device is affected....
The Issue: OmniPods¿ (Pods) have a higher rate of failure causing: Cannula fails to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RadPro 40kW Digital X-Ray Panel and Mobile/Portable Diagnostic X-Ray....
The Issue: Electrostatic energy may be stored in Systems that can cause a short-cicuit...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Etac Relax wall mounted shower seat The Etac Relax is Recalled by Etac...
The Issue: The recalling firm has received reports of a malfunction of the Relax wall...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stryker Sustainability Solutions CB5LT Ethicon Endo-Surgery Recalled by...
The Issue: Stryker Sustainability Solutions has received reports indicating that...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Recalled by GE Healthcare Due to A gradient cable in the ACGD...
The Issue: A gradient cable in the ACGD cabinet may be missing a spacer that prevents...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Perfectum Tuberculin Glass Syringe Recalled by Cadence Inc. Due to...
The Issue: Graduation marks of the syringe are not centered with the numeric position...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Micro-Mate Tuberculin Glass Syringe Recalled by Cadence Inc. Due to...
The Issue: Graduation marks of the syringe are not centered with the numeric position...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medline Electrical Clipper with Charging base The Electrical Surgical...
The Issue: Charging base of surgical clippers overheats and smokes.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Magic3 Hydrophilic-coated Female Intermittent Urinary Catheter 14 Fr in the...
The Issue: Potential breach of the sterile barrier packaging.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Magic3 Hydrophilic-coated Female Intermittent Urinary Catheters (6")...
The Issue: Potential breach of the sterile barrier packaging.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Magic3 Hydrophilic-coated Female Intermittent Urinary Catheters (6")...
The Issue: Potential breach of the sterile barrier packaging.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Magic3 Hydrophilic-coated Female Intermittent Urinary Catheters (6")...
The Issue: Potential breach of the sterile barrier packaging.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Magic3 Hydrophilic-coated Female Intermittent Urinary Catheters (6")...
The Issue: Potential breach of the sterile barrier packaging.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: S4C Occiput Torque Wrench F/Set Screw Recalled by Aesculap, Inc. Due to A...
The Issue: A FW103R torque wrench that was improperly reassembled after reprocessing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RadiForce RX850 Recalled by Eizo Corporation Due to EIZO is recalling the...
The Issue: EIZO is recalling the RadiForce LCD Monitors could display abnormally while...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RadiForce GX540 Recalled by Eizo Corporation Due to EIZO is recalling the...
The Issue: EIZO is recalling the RadiForce LCD Monitors could display abnormally while...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: RadiForce RX650 Recalled by Eizo Corporation Due to EIZO is recalling the...
The Issue: EIZO is recalling the RadiForce LCD Monitors could display abnormally while...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Infant Heel Warmer and Infant Gel Warmer Recalled by CooperSurgical, Inc....
The Issue: Product marketed without a 510(k)
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SENSE Body Coil 1.5T with identification Recalled by Philips Electronics...
The Issue: Wrong positioning of the coil cables can create unintended resonances via...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.