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. 2,367 recalls have been distributed to New Hampshire in the last 12 months.
Showing 25181–25200 of 49,311 recalls
Recalled Item: Acetylcysteine for Injection 6 g/30 mL (200 mg/mL). Rx Only. Recalled by...
The Issue: CGMP Deviations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: ARTIS Pheno Model 10849000. Interventional Fluoroscopic X-Ray System Product...
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: Aplicare Povidone Iodine Prep Pads packaged within Portex Pro-Vent 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: 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: 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: 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: 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: 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: 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.