Product Recalls in North Dakota

Product recalls affecting North Dakota — including food, drugs, consumer products, medical devices, and vehicles distributed to North Dakota. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,503 recalls have been distributed to North Dakota in the last 12 months.

47,938 total recalls
2,503 in last 12 months

Showing 1226112280 of 27,512 recalls

Medical DeviceDecember 19, 2019· Zimmer Biomet, Inc.

Recalled Item: ASI 2.0 Calcar Trimmer Shaft for Use with Zimmer Rasp Recalled by Zimmer...

The Issue: Potential issue associated with the instrument -end of the shaft could fail...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 19, 2019· Philips Medical Systems Gmbh, DMC

Recalled Item: CombiDiagnost GCF Recalled by Philips Medical Systems Gmbh, DMC Due to When...

The Issue: When using the Table Up/Down button, the system may experience Error 80,...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 19, 2019· Intuitive Surgical, Inc.

Recalled Item: STAINLESS STEEL REPROCESSING TRAY Recalled by Intuitive Surgical, Inc. Due...

The Issue: Small but detectable holes in the sterilization wrap used with the firm's 8...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 19, 2019· Intuitive Surgical, Inc.

Recalled Item: STAINLESS STEEL REPROCESSING TRAY Recalled by Intuitive Surgical, Inc. Due...

The Issue: Small but detectable holes in the sterilization wrap used with the firm's 8...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 19, 2019· Philips Medical Systems Gmbh, DMC

Recalled Item: CombiDiagnost PCF Recalled by Philips Medical Systems Gmbh, DMC Due to When...

The Issue: When using the Table Up/Down button, the system may experience Error 80,...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 18, 2019· Covidien LLC

Recalled Item: Polysorb Braided Absorbable Suture 6/0 18" UNDYED P-10 Recalled by Covidien...

The Issue: There is a potential for packaging integrity issues impacting the humidity...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 18, 2019· Covidien LLC

Recalled Item: Polysorb Braided Absorbable Suture 2/0 30"VIOLET GU-46 Recalled by Covidien...

The Issue: There is a potential for packaging integrity issues impacting the humidity...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 18, 2019· Covidien LLC

Recalled Item: Polysorb Braided Absorbable Suture 0 36 VIOLET GS-24 Recalled by Covidien...

The Issue: There is a potential for packaging integrity issues impacting the humidity...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 18, 2019· Covidien LLC

Recalled Item: Polysorb Braided Absorbable Suture 0 30" VIOLET GU-46 Recalled by Covidien...

The Issue: There is a potential for packaging integrity issues impacting the humidity...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 18, 2019· Covidien LLC

Recalled Item: Polysorb Braided Absorbable Suture 0 VIOLET 30" V-20 Recalled by Covidien...

The Issue: There is a potential for packaging integrity issues impacting the humidity...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 18, 2019· Siemens Healthcare Diagnostics, Inc.

Recalled Item: Dimension Enzymatic Creatinine (EZCR) reagent Recalled by Siemens Healthcare...

The Issue: There is a potential for falsely depressed creatinine results for patients...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 18, 2019· Siemens Healthcare Diagnostics, Inc.

Recalled Item: ADVIA Chemistry Enzymatic Creatinine (ECRE_2) reagent Recalled by Siemens...

The Issue: There is a potential for falsely depressed creatinine results for patients...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 18, 2019· Covidien LLC

Recalled Item: Polysorb Braided Absorbable Suture 1 36 VIOLET GS-24 Recalled by Covidien...

The Issue: There is a potential for packaging integrity issues impacting the humidity...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 18, 2019· Covidien LLC

Recalled Item: Polysorb Braided Absorbable Suture 3/0 VIOLET 30" CV-24 (75CM) Recalled by...

The Issue: There is a potential for packaging integrity issues impacting the humidity...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 18, 2019· Covidien LLC

Recalled Item: Polysorb Braided Absorbable Suture 2/0 UNDYED 30" V-30 (75CM) Recalled by...

The Issue: There is a potential for packaging integrity issues impacting the humidity...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 18, 2019· Covidien LLC

Recalled Item: Polysorb Braided Absorbable Suture 4/0 30 VIOLET CVF23 Recalled by Covidien...

The Issue: There is a potential for packaging integrity issues impacting the humidity...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 18, 2019· Covidien LLC

Recalled Item: Polysorb Braided Absorbable Suture UD 4/0 18 P-13 Recalled by Covidien LLC...

The Issue: There is a potential for packaging integrity issues impacting the humidity...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 18, 2019· Covidien LLC

Recalled Item: Polysorb Braided Absorbable Suture 2 36" VIOLET GS-24 Recalled by Covidien...

The Issue: There is a potential for packaging integrity issues impacting the humidity...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 18, 2019· Covidien LLC

Recalled Item: Polysorb Braided Absorbable Suture 2-0 UNDYED 36" GS-21 Recalled by Covidien...

The Issue: There is a potential for packaging integrity issues impacting the humidity...

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

Class II — Potential Health HazardOngoing
Medical DeviceDecember 18, 2019· Covidien LLC

Recalled Item: Polysorb Braided Absorbable Suture 6/0 12"" VL SS-24 D/A Recalled by...

The Issue: There is a potential for packaging integrity issues impacting the humidity...

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

Class II — Potential Health HazardOngoing