Product Recalls in Missouri

Product recalls affecting Missouri — including food, drugs, consumer products, medical devices, and vehicles distributed to Missouri. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 944 recalls have been distributed to Missouri in the last 12 months.

52,570 total recalls
944 in last 12 months

Showing 45401–45420 of 52,570 recalls

Medical DeviceNovember 22, 2013· Smiths Medical ASD, Inc.

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.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 22, 2013· Smiths Medical ASD, Inc.

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.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 22, 2013· Smiths Medical ASD, Inc.

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.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 22, 2013· Smiths Medical ASD, Inc.

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.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 22, 2013· Smiths Medical ASD, Inc.

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.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 22, 2013· Smiths Medical ASD, Inc.

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.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 22, 2013· Smiths Medical ASD, Inc.

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.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 22, 2013· Smiths Medical ASD, Inc.

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.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 22, 2013· Smiths Medical ASD, Inc.

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.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 22, 2013· Smiths Medical ASD, Inc.

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.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 22, 2013· Bio-Rad Laboratories, Inc.

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.

Class III — Low RiskOngoing
Medical DeviceNovember 22, 2013· Smiths Medical ASD, Inc.

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.

Class II — Potential Health HazardOngoing
Medical DeviceNovember 22, 2013· Smiths Medical ASD, Inc.

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.

Class II — Potential Health HazardOngoing
DrugNovember 22, 2013· Faria Limited LLC dba Sheffield Pharmaceuticals

Recalled Item: FAMILY wellness Triple Antibiotic Ointment. NET WT 1 OZ (28 g) Recalled by...

The Issue: Microbial Contamination of Non-Sterile Products: Elevated counts of gram...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 22, 2013· Physicians Total Care, Inc.

Recalled Item: Carisoprodol IV ( Carisoprodol Tablets USP) 350mg Recalled by Physicians...

The Issue: Presence of Foreign Substance; heavy metals (chromium, titanium etc) and...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 22, 2013· Faria Limited LLC dba Sheffield Pharmaceuticals

Recalled Item: Dr. Sheffield Triple Antibiotic Ointment Recalled by Faria Limited LLC dba...

The Issue: Microbial Contamination of Non-Sterile Products: Elevated counts of gram...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 22, 2013· Faria Limited LLC dba Sheffield Pharmaceuticals

Recalled Item: Dollar General Triple Antibiotic Ointment Recalled by Faria Limited LLC dba...

The Issue: Microbial Contamination of Non-Sterile Products: Elevated counts of gram...

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

Class II — Potential Health HazardOngoing
Refund
DrugNovember 21, 2013· Baxter Healthcare Corp.

Recalled Item: 0.9% Sodium Chloride Injection Recalled by Baxter Healthcare Corp. Due to...

The Issue: Presence of Particulate Matter: Baxter is issuing a voluntary recall for...

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

Class I — Serious Health HazardOngoing
Refund
DrugNovember 21, 2013· B. Braun Medical Inc

Recalled Item: Ceftriaxone for Injection and Dextrose Injection 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.

Class I — Serious Health HazardOngoing
Refund
DrugNovember 21, 2013· B. Braun Medical Inc

Recalled Item: Hyperlyte CR (Multi-Electrolyte Concentrate) 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.

Class I — Serious Health HazardOngoing
Refund