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. 2,655 recalls have been distributed to Delaware in the last 12 months.
Showing 7401–7420 of 27,373 recalls
Recalled Item: GentleWave System Posterior CleanFlow Procedure Instrument with Matrices...
The Issue: Procedure Instruments with erroneous unit carton labels.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Laser System Recalled by Spectranetics Corporation Due to Laser...
The Issue: Laser System may detect Error 106 or Error 108 System Failures that will...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BD Phoenix PMIC/ID-107: The Phoenix PMIC/ID panel is used for Recalled by...
The Issue: Misformulated minocycline-can cause erroneously increased Minimal Inhibitory...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS Chemistry Products Calibrator Kit 9 -(GEN) 22 of VITROS Recalled by...
The Issue: Calibration disk Data Release Version (DRV) 6194 to 6200 contain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BASIN SET Recalled by American Contract Systems, Inc. Due to Basin Set...
The Issue: Basin Set labeling error: components within the kit are for the Single Basin...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OneLIF Torque Limiting Adapter Recalled by Novapproach Spine LLC Due to The...
The Issue: The torque limiting adapter may not stay locked inside of the ratcheting...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Superion¿ Indirect Decompression System (IDS) Model Numbers and Size:...
The Issue: Due to Indirect Decompression System devices exhibiting a potential for weld...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hologic Sizer Set- sterilization tray and 6 individual sizers Recalled by...
The Issue: IFU was not provided with the Sizer Set sterilization tray Revised...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CAIRE Liberator 45 Recalled by Caire, Inc. Due to An audit discovered some...
The Issue: An audit discovered some inconsistencies in weld penetration on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CAIRE Liberator 20 Recalled by Caire, Inc. Due to An audit discovered some...
The Issue: An audit discovered some inconsistencies in weld penetration on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CAIRE Liberator 30 Recalled by Caire, Inc. Due to An audit discovered some...
The Issue: An audit discovered some inconsistencies in weld penetration on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CAIRE Liberator 45 Recalled by Caire, Inc. Due to An audit discovered some...
The Issue: An audit discovered some inconsistencies in weld penetration on the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PAJUNK Continuous Epidural Tray Recalled by Pajunk Medical Systems, L.P. Due...
The Issue: The tray contains a 2ml ampule of 0.75% Marcaine Spinal in lieu of a 10ml...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ORISE Gel Submucosal Lifting Agent--Indicated for use in gastrointestinal...
The Issue: ***Update12/13/22***:Product removal due to higher incidence of adverse...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ORISE Gel Syringe Submucosal Lifting Agent Kits: indicated for use Recalled...
The Issue: ***Update12/13/22***:Product removal due to higher incidence of adverse...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ORISE ProKnife Procedure Kits: indicated for use in gastrointestinal...
The Issue: ***Update12/13/22***:Product removal due to higher incidence of adverse...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: FERNO POWER X1 AMBULANCE COT- Item #0015807/UDI-DI 00190790002183 with 36V...
The Issue: Batteries could become unstable when not properly maintained and/or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fogarty Arterial Embolectomy Catheters Model Number: 120602FP 120403FP...
The Issue: Due to an increase of confirmed latex deterioration complaints for arterial...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Fogarty Biliary Balloon Probes Model Number: 410235FP 410405FP 410236FP...
The Issue: Due to an increase of confirmed latex deterioration complaints for arterial...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MicroScan autoSCAN-4 Instrument Recalled by Beckman Coulter, Inc. Due to Due...
The Issue: Due to MicroScan autoSCAN-4 Instruments being manufactured with an incorrect...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.