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. 2,457 recalls have been distributed to Delaware in the last 12 months.
Showing 26541–26560 of 27,373 recalls
Recalled Item: KIT Recalled by Intuitive Surgical, Inc. Due to Specific lots of the...
The Issue: Specific lots of the Instrument Arm Drapes were manufactured with a sterile...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: INSTRUMENT ARM DRAPE IS2000 Recalled by Intuitive Surgical, Inc. Due to...
The Issue: Specific lots of the Instrument Arm Drapes were manufactured with a sterile...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The NCB Polyaxial Locking Plate System NCB screws 26mm: 02.03155.026...
The Issue: Zimmer investigation following a complaint found one lot of NCB Polyaxial...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ACCESSORY BASE STARTER KIT Recalled by Intuitive Surgical, Inc. Due to...
The Issue: Specific lots of the Instrument Arm Drapes were manufactured with a sterile...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hospira LifeShield Latex-Free 100 mL Burette Set Recalled by Hospira Inc....
The Issue: The float valve in the burette sticks to the burette wall and does not open...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: syngo Dynamics Version 9.5 Recalled by Siemens Medical Solutions, USA, Inc...
The Issue: If multiple uncompressed images/clips are sent to the syngo Dynamics server,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KIT Recalled by Intuitive Surgical, Inc. Due to Specific lots of the...
The Issue: Specific lots of the Instrument Arm Drapes were manufactured with a sterile...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Oto Ease by Westone Recalled by Westone Laboratories, Inc. Due to Westone is...
The Issue: Westone is recalling all Oto Ease ear lubricant in all packaging...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AUTOMIX High Speed Compounder System Recalled by Baxter Healthcare Corp. Due...
The Issue: After fluid ingress into the keypad of the AUTOMIX Compounder's (AUTOMIX)...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Recalled by GE Healthcare, LLC Due to GE Healthcare has...
The Issue: GE Healthcare has recently become aware that during use of the Voluson E6 or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Alere Triage TOX Drug Screen 9 Panel Recalled by Alere San Diego, Inc. Due...
The Issue: Alere San Diego is recalling Alere Triage TOX Drug Screen because there is a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Recalled by GE Healthcare, LLC Due to GE Healthcare has...
The Issue: GE Healthcare has recently become aware of a number of potential issues...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Aesculap SIBD 4 degree Trial Implant (SJ768T-US) and Aesculap SIBD Recalled...
The Issue: The 4 degree and 9 degree trial instruments (SJ768T-US/SJ780T-US) are...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips MultiDiagnost Eleva with Flat Detector (MD Eleva FD)Model: 708034...
The Issue: When doing a 3 Dimensional Rotational Angiography (3DRA) the 3D...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Straumann Narrow CrossFit (NC) Screw for CARES Abutment ZrO2. Endosseous...
The Issue: Incorrect Screw (RC) included with NC CARES Abutment Set was not a Narrow...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Breath Tech Recalled by Ventlab Corporation Due to Possible volume leakage...
The Issue: Possible volume leakage through the inlet valve during compressions of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Safe Spot Infant Resuscitator Recalled by Ventlab Corporation Due to...
The Issue: Possible volume leakage through the inlet valve during compressions of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Safe Spot Infant Resuscitator Recalled by Ventlab Corporation Due to...
The Issue: Possible volume leakage through the inlet valve during compressions of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AirFlow Resuscitator Recalled by Ventlab Corporation Due to Possible volume...
The Issue: Possible volume leakage through the inlet valve during compressions of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: V*Care Resuscitator Infant Resuscitator Recalled by Ventlab Corporation Due...
The Issue: Possible volume leakage through the inlet valve during compressions of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.