Product Recalls in New Hampshire
Product recalls affecting New Hampshire — including food, drugs, consumer products, medical devices, and vehicles distributed to New Hampshire. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,471 recalls have been distributed to New Hampshire in the last 12 months.
Showing 15521–15540 of 27,899 recalls
Recalled Item: QUIKFLAP Recalled by Stryker Leibinger GmbH & Co. KG Due to After a three...
The Issue: After a three year term, there is a potential for the external packaging...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: QUIKFLAP Recalled by Stryker Leibinger GmbH & Co. KG Due to After a three...
The Issue: After a three year term, there is a potential for the external packaging...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AXS PP Recalled by Stryker Leibinger GmbH & Co. KG Due to After a three year...
The Issue: After a three year term, there is a potential for the external packaging...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: QUIKFLAP Recalled by Stryker Leibinger GmbH & Co. KG Due to After a three...
The Issue: After a three year term, there is a potential for the external packaging...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: QUIKFLAP Recalled by Stryker Leibinger GmbH & Co. KG Due to After a three...
The Issue: After a three year term, there is a potential for the external packaging...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: QUIKFLAP Recalled by Stryker Leibinger GmbH & Co. KG Due to After a three...
The Issue: After a three year term, there is a potential for the external packaging...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AXS PP Recalled by Stryker Leibinger GmbH & Co. KG Due to After a three year...
The Issue: After a three year term, there is a potential for the external packaging...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AXS PP Recalled by Stryker Leibinger GmbH & Co. KG Due to After a three year...
The Issue: After a three year term, there is a potential for the external packaging...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Artis Q. angiography system. Model 10848280 Recalled by Siemens Medical...
The Issue: Potential hardware issue which may cause thermal effects and possible damage...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AXS PP Recalled by Stryker Leibinger GmbH & Co. KG Due to After a three year...
The Issue: After a three year term, there is a potential for the external packaging...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: QUIKFLAP Recalled by Stryker Leibinger GmbH & Co. KG Due to After a three...
The Issue: After a three year term, there is a potential for the external packaging...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Aplicare Povidone Iodine Prep Pads packaged within Portex Pulsator Arterial...
The Issue: The povidone iodine prep pads packaged with the arterial blood sampling kits...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medtronic EnTrust SingleChamber Implantable Cardioverter Defibrillator with...
The Issue: Medtronic has become aware of a potential for loss of high voltage and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Temperature sensing catheter 18FR Recalled by Degania Silicone, Ltd. Due to...
The Issue: The catheters are suspected to contain defective sensors; if used, defective...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Temperature sensing catheter 16FR Recalled by Degania Silicone, Ltd. Due to...
The Issue: The catheters are suspected to contain defective sensors; if used, defective...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Foley Catheter with temperature sensor 400TM 8FR Recalled by Degania...
The Issue: The catheters are suspected to contain defective sensors; if used, defective...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Foley Temperature Sensor Catheter 12FR Recalled by Degania Silicone, Ltd....
The Issue: The catheters are suspected to contain defective sensors; if used, defective...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Temperature Sensing 100% Silicone Foley Catheter Recalled by Degania...
The Issue: The catheters are suspected to contain defective sensors; if used, defective...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Foley Temperature Sensor Catheter 14FR Recalled by Degania Silicone, Ltd....
The Issue: The catheters are suspected to contain defective sensors; if used, defective...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Temperature Sensor Catheter 14FR Recalled by Degania Silicone, Ltd. Due to...
The Issue: The catheters are suspected to contain defective sensors; if used, defective...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.