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. 2,409 recalls have been distributed to New Hampshire in the last 12 months.

49,311 total recalls
2,409 in last 12 months

Showing 1938119400 of 49,311 recalls

Medical DeviceDecember 17, 2019· Vitreq Bv

Recalled Item: VitreQ 23G Pick Needles-.D04 GTIN: 8719214221584 Recalled by Vitreq Bv Due...

The Issue: Microscopic tears of the sterile pouch may compromise sterility

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 17, 2019· Vitreq Bv

Recalled Item: (1) VitreQ 20G BF Blunt Needles-.D51 GTIN: 8719214221089 (2) Recalled by...

The Issue: Microscopic tears of the sterile pouch may compromise sterility

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 17, 2019· Vitreq Bv

Recalled Item: (1)VitreQ 25G BF Blunt Needles-BF25.D51 GITN: 8719214221164 (2) VitreQ 25G...

The Issue: Microscopic tears of the sterile pouch may compromise sterility

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 17, 2019· Boston Scientific Corporation

Recalled Item: AMS 700 100 mL Recalled by Boston Scientific Corporation Due to A labeling...

The Issue: A labeling discrepancy incorrectly labeled AMS 700 100mL Conceal Low Profile...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 17, 2019· Vitreq Bv

Recalled Item: VitreQ 27G VFI Cannula-.D03 GTIN: 8719214221461 Recalled by Vitreq Bv Due to...

The Issue: Microscopic tears of the sterile pouch may compromise sterility

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 17, 2019· Vitreq Bv

Recalled Item: VitreQ 25G Pick Needles-.D04 GTIN: 8719214221607 Recalled by Vitreq Bv Due...

The Issue: Microscopic tears of the sterile pouch may compromise sterility

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 17, 2019· Vitreq Bv

Recalled Item: VitreQ 25G Silicone Tipped Cannula-.D01 GTIN: 8719214221522 Recalled by...

The Issue: Microscopic tears of the sterile pouch may compromise sterility

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 17, 2019· Vitreq Bv

Recalled Item: VitreQ 27G Blunt Needles with luer-lock connector-.D05 GTIN:8719214221669...

The Issue: Microscopic tears of the sterile pouch may compromise sterility

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 17, 2019· Arthrex, Inc.

Recalled Item: Arthrex Fibulock Fibular Nail Instrument Set Reusable non-sterile...

The Issue: There is a potential for blockage of the Hub Attachment Tube.

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 17, 2019· Vitreq Bv

Recalled Item: VitreQ 25G VFI Cannula-.D03 GTIN: 8719214221447 Recalled by Vitreq Bv Due to...

The Issue: Microscopic tears of the sterile pouch may compromise sterility

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 17, 2019· Vitreq Bv

Recalled Item: VitreQ 25G PFC Injection Needle-.D01 GTIN: 8719214221386 Recalled by Vitreq...

The Issue: Microscopic tears of the sterile pouch may compromise sterility

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 17, 2019· Vitreq Bv

Recalled Item: (1) VitreQ 23G BF Blunt Needles-BF23.D51 GTIN#: 8719214221126 (2) VitreQ...

The Issue: Microscopic tears of the sterile pouch may compromise sterility

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

Class II — Potential Health HazardOngoing
DrugDecember 17, 2019· Hikma Pharmaceuticals USA Inc.

Recalled Item: Ketorolac Tromethamine Injection Recalled by Hikma Pharmaceuticals USA Inc....

The Issue: Presence of Particulate Matter: particles identified as polydimethylsiloxane...

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

Class II — Potential Health HazardOngoing
Refund
DrugDecember 17, 2019· Hikma Pharmaceuticals USA Inc.

Recalled Item: Ketorolac Tromethamine Injection Recalled by Hikma Pharmaceuticals USA Inc....

The Issue: Presence of Particulate Matter: particles identified as polydimethylsiloxane...

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

Class I — Serious Health HazardOngoing
Refund
FoodDecember 17, 2019· TFI Holding dba Grey Ghost Bakery

Recalled Item: GREY GHOST BAKERY scratch-made cookies LEMON SUGAR NET WT 1.4 OZ (40 G)...

The Issue: The product contains undeclared sulfites.

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceDecember 16, 2019· Synthes, Inc.

Recalled Item: 2.4MM TI VA LOCKING SCREW STARDRIVE 24MM STERILE Recalled by Synthes, Inc....

The Issue: There is a possibility that the inner cap could open when the outer cap is...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 16, 2019· GE Healthcare, LLC

Recalled Item: Centricity Universal Viewer 6.0 Recalled by GE Healthcare, LLC Due to...

The Issue: Centricity Universal Viewer measurements saved into a DICOM Grayscale...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 16, 2019· Synthes, Inc.

Recalled Item: 2.4MM TI VA LOCKING SCREW STARDRIVE 12MM STERILE Recalled by Synthes, Inc....

The Issue: There is a possibility that the inner cap could open when the outer cap is...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 16, 2019· Synthes, Inc.

Recalled Item: 2.4MM TI VA LOCKING SCREW STARDRIVE 18MM STERILE Recalled by Synthes, Inc....

The Issue: There is a possibility that the inner cap could open when the outer cap is...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 16, 2019· Ortho Clinical Diagnostics Inc

Recalled Item: VITROS Chemistry Products Calibrator Kit 2- IVD calibrator for VITROS...

The Issue: Potential for Negatively Biased Na+ Urine Results Using Several Lots of...

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

Class II — Potential Health HazardOngoing