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. 2,552 recalls have been distributed to New Hampshire in the last 12 months.

49,311 total recalls
2,552 in last 12 months

Showing 56615680 of 27,899 recalls

Medical DeviceAugust 7, 2023· Stryker Corporation

Recalled Item: Stryker ACM (Advanced Cement Mixing): 180-Gram Cement Cartridge with...

The Issue: Potential for the Break-Away Femoral Nozzle the applicator tip connecting...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 7, 2023· Stryker Corporation

Recalled Item: Stryker ACM (Advanced Cement Mixing) System: ACM Kit w/ Femoral Recalled by...

The Issue: Potential for the Break-Away Femoral Nozzle the applicator tip connecting...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 7, 2023· Stryker Corporation

Recalled Item: Stryker ACM (Advanced Cement Mixing) System: ACM Kit w/ Femoral Recalled by...

The Issue: Potential for the Break-Away Femoral Nozzle the applicator tip connecting...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 7, 2023· Stryker Corporation

Recalled Item: Stryker ACM (Advanced Cement Mixing)System: ACM Kit w/ Femoral Breakaway...

The Issue: Potential for the Break-Away Femoral Nozzle the applicator tip connecting...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 7, 2023· Stryker Corporation

Recalled Item: Stryker ACM (Advanced Cement Mixing)System: ACM Kit w/ Femoral Breakaway...

The Issue: Potential for the Break-Away Femoral Nozzle the applicator tip connecting...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 7, 2023· Stryker Corporation

Recalled Item: Stryker ACM (Advanced Cement Mixing) System: Break-Away Femoral Nozzle-...

The Issue: Potential for the Break-Away Femoral Nozzle the applicator tip connecting...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 7, 2023· Stryker Corporation

Recalled Item: Stryker ACM (Advanced Cement Mixing) System: ACM Kit w/ Femoral Recalled by...

The Issue: Potential for the Break-Away Femoral Nozzle the applicator tip connecting...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 7, 2023· B. Braun Medical, Inc.

Recalled Item: B.Braun NORM-JECT Luer Lock Solo Recalled by B. Braun Medical, Inc. Due to...

The Issue: The sterile blister packaging may be damaged, and sterility may be compromised

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 7, 2023· B. Braun Medical, Inc.

Recalled Item: B. Braun NORM-JECT Luer Solo Recalled by B. Braun Medical, Inc. Due to The...

The Issue: The sterile blister packaging may be damaged, and sterility may be compromised

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 7, 2023· Thoratec Corp.

Recalled Item: Heartmate 3 LVAS Implant Kit Recalled by Thoratec Corp. Due to Inability to...

The Issue: Inability to start and/or complete the coring procedure due to inadequate...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 5, 2023· Ortho-Clinical Diagnostics, INc.

Recalled Item: VITROS XT Chemistry Products TBIL-ALKP Slides Recalled by Ortho-Clinical...

The Issue: Samples containing high levels of ALKP (or an interfering substance) could...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 5, 2023· Ortho-Clinical Diagnostics, INc.

Recalled Item: VITROS XT Chemistry Products ALKP Slides Recalled by Ortho-Clinical...

The Issue: Samples containing high levels of ALKP (or an interfering substance) could...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 4, 2023· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: HUDSON RCI Addipak Recalled by MEDLINE INDUSTRIES, LP - Northfield Due to...

The Issue: Product dispositioned for scrap for sterility failure investigation that was...

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

Class I — Serious Health HazardOngoing
Medical DeviceAugust 3, 2023· Accuray Incorporated

Recalled Item: Upper roller bracket (part number 1088370) for the Gen2 gantry Recalled by...

The Issue: It is possible the upper roller bracket in the Radixact System gantry...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 3, 2023· LivaNova Deutschland GmbH

Recalled Item: 3T Heater Cooler System Recalled by LivaNova Deutschland GmbH Due to The...

The Issue: The firm's labeling (Quick Guide) contains incorrect information in the...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 3, 2023· MEDLINE INDUSTRIES, LP - Northfield

Recalled Item: MEDLINE STERILE IRIS SCISSORS CVD/STD Recalled by MEDLINE INDUSTRIES, LP -...

The Issue: 4.5" Iris Scissors, Sterile, Curved (DYNJ04049) are being recalled due to...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 3, 2023· Ansell Healthcare Products LLC

Recalled Item: NOVAPLUS GAMMEX NON-LATEX PI GREEN Surgical gloves Recalled by Ansell...

The Issue: Some surgical glove sterile pouches were not completely sealed.

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 3, 2023· Ansell Healthcare Products LLC

Recalled Item: GAMMEX NON-LATEX PI GREEN Surgical gloves Recalled by Ansell Healthcare...

The Issue: Some surgical glove sterile pouches were not completely sealed.

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 2, 2023· Philips Healthcare

Recalled Item: Incisive CT Recalled by Philips Healthcare Due to Philips has identified...

The Issue: Philips has identified three software issues with compliance concerns to...

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

Class II — Potential Health HazardOngoing
Medical DeviceAugust 1, 2023· Skytron, LLC

Recalled Item: GS70 Salus Surgical Table Recalled by Skytron, LLC Due to When the control...

The Issue: When the control of the operating table was used in Bluetooth mode, the...

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

Class II — Potential Health HazardOngoing