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. 1,757 recalls have been distributed to Missouri in the last 12 months.
Showing 43841–43860 of 52,570 recalls
Recalled Item: Cottage Doubles - cottage cheese Recalled by Kraft Foods Group Due to Kraft...
The Issue: Kraft Foods is voluntarily recalling 18 SKUs of Knudsen Cottage Cheese, nine...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Cottage Doubles - cottage cheese Recalled by Kraft Foods Group Due to Kraft...
The Issue: Kraft Foods is voluntarily recalling 18 SKUs of Knudsen Cottage Cheese, nine...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Fat free cottage cheese sold under the Knudsen or Kraft Recalled by Kraft...
The Issue: Kraft Foods is voluntarily recalling 18 SKUs of Knudsen Cottage Cheese, nine...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Low fat cottage cheese Recalled by Kraft Foods Group Due to Kraft Foods is...
The Issue: Kraft Foods is voluntarily recalling 18 SKUs of Knudsen Cottage Cheese, nine...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Low fat cottage cheese Recalled by Kraft Foods Group Due to Kraft Foods is...
The Issue: Kraft Foods is voluntarily recalling 18 SKUs of Knudsen Cottage Cheese, nine...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Labetalol Hydrochloride Injection Recalled by Hospira Inc. Due to Presence...
The Issue: Presence of Particulate Matter; metal embedded in the glass vial and visible...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: ePHEDrine Sulfate Injection Recalled by US Compounding Inc Due to Mislabeling
The Issue: Labeling: Label Error on Declared Strength; The outer light protective bags,...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Vancomycin Hydrochloride Capsules Recalled by Actavis Inc Due to Subpotent Drug.
The Issue: Subpotent Drug.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: IntellaTip MiFi XP Temperature Ablation Catheter Recalled by Boston...
The Issue: Some units of Intella Tip MiFi XP Temperature Ablation Catheters were not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IntellaTip MiFi XP Temperature Ablation Catheter Recalled by Boston...
The Issue: Some units of Intella Tip MiFi XP Temperature Ablation Catheters were not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IntellaTip MiFi XP Temperature Ablation Catheter Recalled by Boston...
The Issue: Some units of Intella Tip MiFi XP Temperature Ablation Catheters were not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IntellaTip MiFi XP Temperature Ablation Catheter Recalled by Boston...
The Issue: Some units of Intella Tip MiFi XP Temperature Ablation Catheters were not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Biomet Spine Recalled by Ebi, Llc Due to The Cypher MIS Screw Inserter may...
The Issue: The Cypher MIS Screw Inserter may exhibit an increased rate of instrument...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips MR systems: Trolley Variable Height IRF (for Ingenia 1.5T Recalled...
The Issue: Ingenia customers have experienced clamping of the foot under the central...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IntellaTip MiFi XP Temperature Ablation Catheter Recalled by Boston...
The Issue: Some units of Intella Tip MiFi XP Temperature Ablation Catheters were not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DISCOVERY ELBOW prosthesis Recalled by Biomet, Inc. Due to Surface finish is...
The Issue: Surface finish is different than specified. The implant has 30 grit blast on...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens syngo RT Dosimetrist 2.7 system Product Usage: The intended Recalled...
The Issue: An update to the Virtual Simulation software of the syngo RT Dosimetrist is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips MR systems: Ingenia HA FLEX TRAK Trolley (for Ingenia Recalled by...
The Issue: Ingenia customers have experienced clamping of the foot under the central...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Simplexa" Flu A/B & RSV Direct Recalled by Focus Diagnostics Inc Due to...
The Issue: Focus Diagnostics is providing an urgent safety notice for a correction to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synthes B37 Replacement Screws. M3.5 Screw for insertion handle guide/aiming...
The Issue: All lots of B37 Replacement Screws are being recalled due to potential...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.