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. 1,908 recalls have been distributed to North Dakota in the last 12 months.
Showing 12221–12240 of 27,512 recalls
Recalled Item: Prometra Programmable 20mL Pump. Catalog No. 91827 The device is Recalled by...
The Issue: A pump alarm function anomaly in the pump firmware code may result in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Prometra II 20mL Pump. Catalog No. 13827 The device is Recalled by Flowonix...
The Issue: A pump alarm function anomaly in the pump firmware code may result in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Prometra II Programmable 20mL Pump. Catalog No. 93827 The device Recalled by...
The Issue: A pump alarm function anomaly in the pump firmware code may result in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Jamshidi Bone Marrow Aspiration Needle Item Number: 00-1103-007-00 Recalled...
The Issue: Potential for the expiration date on the outer label that was applied by...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SIGNA Pioneer Nuclear Magnetic Resonance Imaging System - Product Usage:...
The Issue: It was identified that due to a potential installation workflow issue, the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MVAP MEDICAL SUPPLIES INC Recalled by Carroll-Baccari, Inc. Due to Samples...
The Issue: Samples of 114gm tubes of Lemon Prep, collected during a Food and Drug...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LemonPrep Tubes (MD0019-T) and Single use cups (MD0019-SUP) Recalled by...
The Issue: Samples of 114gm tubes of Lemon Prep, collected during a Food and Drug...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SIGNA Vibrant Nuclear Magnetic Resonance Imaging System Recalled by GE...
The Issue: It was identified that due to a potential installation workflow issue, the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Nikon Metrology XTH cabinet x-ray Systems which includes variations STH225...
The Issue: The manufacturer identified a risk that their products might fail to comply...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SIGNA Architect Nuclear Magnetic Resonance Imaging System - Product Usage:...
The Issue: It was identified that due to a potential installation workflow issue, the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SIGNA Premier Nuclear Magnetic Resonance Imaging System - Product Usage:...
The Issue: It was identified that due to a potential installation workflow issue, the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Wave Prep Tubes (1710-03) and single use cups (17--00-24) Recalled by...
The Issue: Samples of 114gm tubes of Lemon Prep, collected during a Food and Drug...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VesselNavigator application used with Philips Azurion (Azurion 7 Series)...
The Issue: Due to a software defect, when a digital subtraction angiography (DSA) is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PediaPrep Tubes (MD0033-T) and Single use cups (MD0033-SUP) Recalled by...
The Issue: Samples of 114gm tubes of Lemon Prep, collected during a Food and Drug...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arrow Maximal Barrier Drape ASK-00002-1A Recalled by Arrow International Inc...
The Issue: Product lidstock contains the incorrect expiration date for the product
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arrow EPIDURAL CATHETERIZATION KIT YC-02220 Recalled by Arrow International...
The Issue: Product lidstock contains the incorrect expiration date for the product
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arrow EPIDURAL CATHETERIZATION COMPONENT EC-05000 Recalled by Arrow...
The Issue: Product lidstock contains the incorrect expiration date for the product
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arrow¿ EPIDURAL CATHETERIZATION KIT AK-05000 Recalled by Arrow International...
The Issue: Product lidstock contains the incorrect expiration date for the product
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PICC Set- PR-35052-HPHNM Recalled by Arrow International Inc Due to Product...
The Issue: Product lidstock contains the incorrect expiration date for the product
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arrow FlexTip Plus(R) Epidural Catheterization Kit ASK-05500-CAN Recalled by...
The Issue: Product lidstock contains the incorrect expiration date for the product
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.