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. 2,482 recalls have been distributed to Delaware in the last 12 months.
Showing 21741–21760 of 27,373 recalls
Recalled Item: 1/4 in. Round Drain with Trocar Curved Trocar with Wound Recalled by Stryker...
The Issue: Stryker Instruments is voluntarily recalling the CBCII Wound Drains and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 3/16 in. Curved Trocar with Wound Drain Curved Trocar with Recalled by...
The Issue: Stryker Instruments is voluntarily recalling the CBCII Wound Drains and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: EVIS EXERA II Duodenovideoscope OLYMPUS TJF TypeQ180V. This instrument has...
The Issue: New and validated reprocessing procedures have been issued for the Olympus...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 1/8 in. Double Trocar with Wound Drain Curved Trocar with Recalled by...
The Issue: Stryker Instruments is voluntarily recalling the CBCII Wound Drains and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 1/4 in. Trocar with Single Drain Curved Trocar with Wound Recalled by...
The Issue: Stryker Instruments is voluntarily recalling the CBCII Wound Drains and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 1/4 in. Curved Trocar with Wound Drain Curved Trocar with Recalled by...
The Issue: Stryker Instruments is voluntarily recalling the CBCII Wound Drains and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 1/8 in. Trocar with Single Drain Curved Trocar with Wound Recalled by...
The Issue: Stryker Instruments is voluntarily recalling the CBCII Wound Drains and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CSA Medical truFreeze Console- Cryosurgical Unit Cryogenic Surgical Device...
The Issue: TruFreeze Console caused a higher rate of liquid nitrogen (cryogen) to be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Universal Charger Product Usage: The Stryker Universal Battery Charger is...
The Issue: The Stryker Universal Battery Charger is not transmitting usage data to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Light Sheer Desire Diode Laser System with XC Handpiece Accessory options....
The Issue: Device software treatment preset parameters for the XC treatment handpiece...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TIGERPAW System II Recalled by Laax, Inc. Due to Increase of field reports...
The Issue: Increase of field reports involving issues with the TIGERPAW System II...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TIGERPAW System II Recalled by Laax, Inc. Due to Increase of field reports...
The Issue: Increase of field reports involving issues with the TIGERPAW System II...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hamilton-G5 Ventilators with software versions V2.40/2.41 Catalog numbers...
The Issue: Customer reports that the ventilator display can freeze. Ventilation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synthes Small Battery Drive (SBD) Oscillating Saw Attachment Part Number:...
The Issue: The potential exists for the Oscillating Saw Attachment to disengage from...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Covidien Trellis 6 and Trellis 8 Peripheral Infusion Systems Recalled by...
The Issue: Medtronic is conducting a voluntary recall of all former Covidien Trellis 6...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sedecal SA Mobile Diagnost w DR x-ray system Recalled by Sedecal USA, Inc....
The Issue: Due to a software defect, the system may sporadically apply the default x...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Edwards Lifesciences Fem-Flex II Femoral Arterial Cannula 8 Recalled by...
The Issue: Edwards Lifesciences is recalling Fem-Flex II Pediatric Femoral Arterial...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA Chemistry Lipase Reagent Recalled by Siemens Healthcare Diagnostics,...
The Issue: Siemens internal investigation confirmed that current contamination...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips DigitalDiagnost Release 4.0.3 Recalled by Philips Electronics North...
The Issue: The system is designed to emit a beep upon termination of an exposure....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Homocysteine test system - Homocysteine Reagent. 05385415190 Recalled by...
The Issue: Customers complained about under-recovery of non-Roche controls and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.