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. 2,387 recalls have been distributed to Minnesota in the last 12 months.
Showing 45141–45160 of 52,120 recalls
Recalled Item: 4042LH: 3 mL Line Draw Recalled by Smiths Medical ASD, Inc. Due to issue...
The Issue: issue with the plunger tip of the Portex¿ Arterial Blood Sampling Line Draw...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 4042-2: 3 mL Line Draw Recalled by Smiths Medical ASD, Inc. Due to issue...
The Issue: issue with the plunger tip of the Portex¿ Arterial Blood Sampling Line Draw...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: G1777: Umbilical (2) 3 mL Line Draw Recalled by Smiths Medical ASD, Inc. Due...
The Issue: issue with the plunger tip of the Portex¿ Arterial Blood Sampling Line Draw...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: G2001: 3 mL Line Draw Recalled by Smiths Medical ASD, Inc. Due to issue with...
The Issue: issue with the plunger tip of the Portex¿ Arterial Blood Sampling Line Draw...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 4043G-2: 3 mL Line Draw Recalled by Smiths Medical ASD, Inc. Due to issue...
The Issue: issue with the plunger tip of the Portex¿ Arterial Blood Sampling Line Draw...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 4043E: 3 mL Line Draw Recalled by Smiths Medical ASD, Inc. Due to issue with...
The Issue: issue with the plunger tip of the Portex¿ Arterial Blood Sampling Line Draw...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 4042E: 3 mL Line Draw Recalled by Smiths Medical ASD, Inc. Due to issue with...
The Issue: issue with the plunger tip of the Portex¿ Arterial Blood Sampling Line Draw...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: G1762: 3 mL Line Draw Recalled by Smiths Medical ASD, Inc. Due to issue with...
The Issue: issue with the plunger tip of the Portex¿ Arterial Blood Sampling Line Draw...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: G1725: 3 mL Line Draw Recalled by Smiths Medical ASD, Inc. Due to issue with...
The Issue: issue with the plunger tip of the Portex¿ Arterial Blood Sampling Line Draw...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: G1469J: 3 mL Line Draw Recalled by Smiths Medical ASD, Inc. Due to issue...
The Issue: issue with the plunger tip of the Portex¿ Arterial Blood Sampling Line Draw...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 4040-2: Umbilical 3 mL Line Draw Recalled by Smiths Medical ASD, Inc. Due to...
The Issue: issue with the plunger tip of the Portex¿ Arterial Blood Sampling Line Draw...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 4043W-2: 3 mL Line Draw Recalled by Smiths Medical ASD, Inc. Due to issue...
The Issue: issue with the plunger tip of the Portex¿ Arterial Blood Sampling Line Draw...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 4043-2: 3 mL Line Draw Recalled by Smiths Medical ASD, Inc. Due to issue...
The Issue: issue with the plunger tip of the Portex¿ Arterial Blood Sampling Line Draw...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: D-10 Dual Program Recalled by Bio-Rad Laboratories, Inc. Due to D-10 A1c...
The Issue: D-10 A1c Dual Program Floppy was programmed incorrectly and cartridge...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Medfusion¿ 4000 Syringe Infusion Pumps Medfusion¿ 4000 Syringe Infusion...
The Issue: Smiths Medical is conducting a recall involving all Medfusion¿ 4000 Syringe...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cefoxitin for Injection and Dextrose Injection Recalled by B. Braun Medical...
The Issue: Presence of Particulate Matter: B. Braun Medical Inc. is recalling several...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Cefazolin for Injection USP and Dextrose Injections USP Recalled by B. Braun...
The Issue: Presence of Particulate Matter: B. Braun Medical Inc. is recalling several...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Cefepime for Injections USP and Dextrose Injection USP Recalled by B. Braun...
The Issue: Presence of Particulate Matter: B. Braun Medical Inc. is recalling several...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: 0.9 % Sodium Chloride Injection USP Recalled by B. Braun Medical Inc Due to...
The Issue: Presence of Particulate Matter: B. Braun Medical Inc. is recalling several...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: 0.9 % Sodium Chloride Injection USP in PAB 50 mL Recalled by B. Braun...
The Issue: Presence of Particulate Matter: B. Braun Medical Inc. is recalling several...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.