Product Recalls in Minnesota
Product recalls affecting Minnesota — including food, drugs, consumer products, medical devices, and vehicles distributed to Minnesota. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,693 recalls have been distributed to Minnesota in the last 12 months.
Showing 3261–3280 of 29,186 recalls
Recalled Item: Impella 5.5 with SmartAssist Set Recalled by Abiomed, Inc. Due to A...
The Issue: A potential device interaction between the Shockwave Coronary IVL Catheter...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Impella 5.5 SmartAssist S2 Set Recalled by Abiomed, Inc. Due to A potential...
The Issue: A potential device interaction between the Shockwave Coronary IVL Catheter...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ERIC Retrieval Device ER174030 ER176044 The ERIC Retrieval Recalled by...
The Issue: Due to Retrieval Device product labels stating the incorrect expiration...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Impella CP Smart Assist Set Recalled by Abiomed, Inc. Due to A potential...
The Issue: A potential device interaction between the Shockwave Coronary IVL Catheter...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Impella CP Smart Assist Set Recalled by Abiomed, Inc. Due to A potential...
The Issue: A potential device interaction between the Shockwave Coronary IVL Catheter...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Impella CP Pump 371 Set Recalled by Abiomed, Inc. Due to A potential device...
The Issue: A potential device interaction between the Shockwave Coronary IVL Catheter...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ImpellaCP SmartAssistSetAPAC Recalled by Abiomed, Inc. Due to A potential...
The Issue: A potential device interaction between the Shockwave Coronary IVL Catheter...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Impella CP Smart Assist Set APAC Recalled by Abiomed, Inc. Due to A...
The Issue: A potential device interaction between the Shockwave Coronary IVL Catheter...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Impella 5.5 with SmartAssist Set Recalled by Abiomed, Inc. Due to A...
The Issue: A potential device interaction between the Shockwave Coronary IVL Catheter...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Impella CP Pump Set Recalled by Abiomed, Inc. Due to A potential device...
The Issue: A potential device interaction between the Shockwave Coronary IVL Catheter...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Monarch Platform (Urology) Recalled by AURIS HEALTH INC Due to...
The Issue: Endoscopy/bronchoscopy/urology devices may have a strain relief defect with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Monarch Platform (Endoscopy) Recalled by AURIS HEALTH INC Due to...
The Issue: Endoscopy/bronchoscopy/urology devices may have a strain relief defect with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BARD MAGNUM Disposable Core Tissue Biopsy Needle MN Recalled by Bard...
The Issue: Due to possible packaging damage (indentations/cuts) cause by manufacturing...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Vit-l-escence Product Name: Vit-l-escence Singles A3...
The Issue: Due to a manufacturing issue, red particulates present in the expressed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Transcend Product Name: Transcend Econo Kit (UB) - Recalled by...
The Issue: Due to a manufacturing issue, red particulates present in the expressed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Brand Name: Transcend Product Name: Transcend Singles Universal Body (UB)...
The Issue: Due to a manufacturing issue, red particulates present in the expressed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: WALLFLEX FC ESO STENT RMV LL 23X125-Wallflex Esophageal Partially Covered...
The Issue: WallFlexTM Esophageal Stent System and AgileTM Esophageal Over the Wire...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: WALLFLEX FC ESO STENT RMV LL 23X105- Intended for maintaining Recalled by...
The Issue: WallFlexTM Esophageal Stent System and AgileTM Esophageal Over the Wire...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AGILE ESO OTW FC 23MM X 10.1CM IN 18.5 F-Agile Recalled by Boston Scientific...
The Issue: WallFlexTM Esophageal Stent System and AgileTM Esophageal Over the Wire...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: WALLFLEX FC ESO STENT RMV LL 18X103- Wallflex Esophageal Partially Recalled...
The Issue: WallFlexTM Esophageal Stent System and AgileTM Esophageal Over the Wire...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.