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. 2,540 recalls have been distributed to New Hampshire in the last 12 months.

49,311 total recalls
2,540 in last 12 months

Showing 76417660 of 49,311 recalls

DrugSeptember 21, 2023· Central Admixture Pharmacy Services Inc

Recalled Item: PHENYLephrine in 0.9% sodium chloride Recalled by Central Admixture Pharmacy...

The Issue: Lack of assurance of sterility:

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 21, 2023· Central Admixture Pharmacy Services Inc

Recalled Item: HYDROmorphone in dextrose 5% Recalled by Central Admixture Pharmacy Services...

The Issue: Lack of assurance of sterility:

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 21, 2023· Central Admixture Pharmacy Services Inc

Recalled Item: fentaNYL Recalled by Central Admixture Pharmacy Services Inc Due to Lack of...

The Issue: Lack of assurance of sterility:

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 21, 2023· Central Admixture Pharmacy Services Inc

Recalled Item: lidocaine 2% Recalled by Central Admixture Pharmacy Services Inc Due to Lack...

The Issue: Lack of assurance of sterility:

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 21, 2023· Central Admixture Pharmacy Services Inc

Recalled Item: HYDROmorphone in 0.9% Sodium Chloride Recalled by Central Admixture Pharmacy...

The Issue: Lack of assurance of sterility:

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 21, 2023· Central Admixture Pharmacy Services Inc

Recalled Item: ePHEDrine in 0.9% sodium chloride Recalled by Central Admixture Pharmacy...

The Issue: Lack of assurance of sterility:

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 21, 2023· Central Admixture Pharmacy Services Inc

Recalled Item: rocuronium Recalled by Central Admixture Pharmacy Services Inc Due to Lack...

The Issue: Lack of assurance of sterility:

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 21, 2023· Central Admixture Pharmacy Services Inc

Recalled Item: fentaNYL in 0.9% sodium chloride Recalled by Central Admixture Pharmacy...

The Issue: Lack of assurance of sterility:

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
DrugSeptember 21, 2023· Central Admixture Pharmacy Services Inc

Recalled Item: HYDROmorphone in dextrose 5% Recalled by Central Admixture Pharmacy Services...

The Issue: Lack of assurance of sterility:

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceSeptember 21, 2023· Philips North America Llc

Recalled Item: DigitalDiagnost 4 Chest/Emergency Recalled by Philips North America Llc Due...

The Issue: Potential for units suspended on the ceiling to fail and fall.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 21, 2023· Philips North America Llc

Recalled Item: CombiDiagnost R90 Recalled by Philips North America Llc Due to Potential for...

The Issue: Potential for units suspended on the ceiling to fail and fall.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 21, 2023· Philips North America Llc

Recalled Item: DigitalDiagnost 4 High Performance Recalled by Philips North America Llc Due...

The Issue: Potential for units suspended on the ceiling to fail and fall.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 21, 2023· Philips North America Llc

Recalled Item: DigitalDiagnost C90 Release 3 Recalled by Philips North America Llc Due to...

The Issue: Potential for units suspended on the ceiling to fail and fall.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 21, 2023· Philips North America Llc

Recalled Item: DigitalDiagnost C90 Release 3.1 Recalled by Philips North America Llc Due to...

The Issue: Potential for units suspended on the ceiling to fail and fall.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 21, 2023· Philips North America Llc

Recalled Item: ProxiDiagnost N90 Recalled by Philips North America Llc Due to Potential for...

The Issue: Potential for units suspended on the ceiling to fail and fall.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 21, 2023· Philips North America Llc

Recalled Item: DigitalDiagnost C90 High Performance Recalled by Philips North America Llc...

The Issue: Potential for units suspended on the ceiling to fail and fall.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 21, 2023· Philips North America Llc

Recalled Item: DigitalDiagnost C90 Flex/Value/Chest/ER Recalled by Philips North America...

The Issue: Potential for units suspended on the ceiling to fail and fall.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 21, 2023· Philips North America Llc

Recalled Item: EasyDiagnost Eleva DRF Recalled by Philips North America Llc Due to...

The Issue: Potential for units suspended on the ceiling to fail and fall.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 21, 2023· Philips North America Llc

Recalled Item: DigitalDiagnost 4 Flex/Value Recalled by Philips North America Llc Due to...

The Issue: Potential for units suspended on the ceiling to fail and fall.

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceSeptember 21, 2023· B. Braun Medical, Inc.

Recalled Item: 8713051U Recalled by B. Braun Medical, Inc. Due to Upstream occlusion alarm...

The Issue: Upstream occlusion alarm may sound when no occlusion exists, and the device...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing