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. 2,422 recalls have been distributed to Minnesota in the last 12 months.

52,120 total recalls
2,422 in last 12 months

Showing 4036140380 of 52,120 recalls

Medical DeviceApril 13, 2015· The Anspach Effort, Inc.

Recalled Item: ANSPACH - 6MM Coarse Diamond Ball Recalled by The Anspach Effort, Inc. Due...

The Issue: G1 Dissection Tools are not compatible with all attachments listed on the...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 13, 2015· The Anspach Effort, Inc.

Recalled Item: ANSPACH -3MM Coarse Diamond Ball Recalled by The Anspach Effort, Inc. Due to...

The Issue: G1 Dissection Tools are not compatible with all attachments listed on the...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 13, 2015· The Anspach Effort, Inc.

Recalled Item: ANSPACH - 3MM Fluted Ball Recalled by The Anspach Effort, Inc. Due to G1...

The Issue: G1 Dissection Tools are not compatible with all attachments listed on the...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 13, 2015· The Anspach Effort, Inc.

Recalled Item: ANSPACH - 5MM x 11.3MM Fluted Barrel Recalled by The Anspach Effort, Inc....

The Issue: G1 Dissection Tools are not compatible with all attachments listed on the...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 13, 2015· The Anspach Effort, Inc.

Recalled Item: ANSPACH - 5MM Fluted Ball Recalled by The Anspach Effort, Inc. Due to G1...

The Issue: G1 Dissection Tools are not compatible with all attachments listed on the...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 13, 2015· The Anspach Effort, Inc.

Recalled Item: ANSPACH - Fluted Drum Recalled by The Anspach Effort, Inc. Due to G1...

The Issue: G1 Dissection Tools are not compatible with all attachments listed on the...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 13, 2015· CooperSurgical, Inc.

Recalled Item: McKesson Medi-Pak Vaginal Speculum Recalled by CooperSurgical, Inc. Due to...

The Issue: Small sized specula were incorrectly packaged in printed bags for the medium...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 13, 2015· Siemens Medical Solutions USA, Inc

Recalled Item: SIEMENS Ysio Max Recalled by Siemens Medical Solutions USA, Inc Due to Study...

The Issue: Study and all acquired images deleted when using systems with software...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 13, 2015· Siemens Medical Solutions USA, Inc

Recalled Item: SIEMENS Luminos Agile Max Recalled by Siemens Medical Solutions USA, Inc Due...

The Issue: Study and all acquired images deleted when using systems with software...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 13, 2015· Siemens Medical Solutions USA, Inc

Recalled Item: SIEMENS Axiom Luminos dRF Max Recalled by Siemens Medical Solutions USA, Inc...

The Issue: Study and all acquired images deleted when using systems with software...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 13, 2015· Siemens Medical Solutions USA, Inc

Recalled Item: SIEMENS Uroskop Omnia Max Recalled by Siemens Medical Solutions USA, Inc Due...

The Issue: Study and all acquired images deleted when using systems with software...

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

Class II — Potential Health HazardOngoing
DrugApril 12, 2015· Stroheckers Inc Pharmacy

Recalled Item: Testosterone Cypionate 200 mg/mL in Sesame oil Recalled by Stroheckers Inc...

The Issue: Incorrect Product Formulation: Vials labeled as Testosterone Cypionate 200...

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

Class I — Serious Health HazardOngoing
Refund
DrugApril 10, 2015· Medtech Products, Inc.

Recalled Item: MONISTAT 1 SIMPLE CURE (Miconazole Nitrate Vaginal Insert) 1200 mg ovule...

The Issue: Marketed without an approved NDA/ANDA: The distributed units of Monistat 1...

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

Class III — Low RiskOngoing
Refund
Medical DeviceApril 10, 2015· Medtronic Neuromodulation

Recalled Item: Medtronic SynchroMed II Implantable Infusion Pumps Recalled by Medtronic...

The Issue: Medtronic is conducting a recall of a specific subset of Model 8637-20 and...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 10, 2015· Philips Ultrasound, Inc.

Recalled Item: EPIQ 7 Ultrasound System with Pediatric Cardiology option Recalled by...

The Issue: When Epiq 7 Ultrasound System, WITH the Pediatric Cardiology option, is set...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 10, 2015· Philips Ultrasound, Inc.

Recalled Item: EPIQ 5 Ultrasound System with Pediatric Cardiology option Recalled by...

The Issue: When Epiq 5 Ultrasound System, WITH the Pediatric Cardiology option, is set...

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

Class II — Potential Health HazardOngoing
FoodApril 9, 2015· New Punjab Sweets Inc.

Recalled Item: New Punjab Kaju (Kajoo) Fry is the Indian translation for Recalled by New...

The Issue: This voluntary recall is being initiated because the following Indian snack...

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

Class II — Potential Health HazardOngoing
Refund
FoodApril 9, 2015· New Punjab Sweets Inc.

Recalled Item: New Punjab Kaju Roll is an Indian snack cut into Recalled by New Punjab...

The Issue: This voluntary recall is being initiated because the following Indian snack...

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

Class II — Potential Health HazardOngoing
Refund
FoodApril 9, 2015· New Punjab Sweets Inc.

Recalled Item: New Punjab Kaju Katri is an Indian snack cut into Recalled by New Punjab...

The Issue: This voluntary recall is being initiated because the following Indian snack...

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

Class II — Potential Health HazardOngoing
Refund
FoodApril 9, 2015· New Punjab Sweets Inc.

Recalled Item: New Punjab Chum Chum is a oval-shaped Indian snack coated Recalled by New...

The Issue: This voluntary recall is being initiated because the following Indian snack...

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

Class II — Potential Health HazardOngoing
Refund