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. 2,695 recalls have been distributed to Missouri in the last 12 months.
Showing 4341–4360 of 52,570 recalls
Recalled Item: Ascorbic Acid Inj. Solution Recalled by Staska Pharmaceuticals, Inc. Due to...
The Issue: Presence of Particulate Matter: Presence of glass particulates.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Ciclopirox Gel 0.77% Recalled by Glenmark Pharmaceuticals Inc., USA Due to...
The Issue: Defective Container: Firm received complaints of broken tube at the seal.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Bard Marquee Disposable Core Biopsy Instrument Kit: BARD MARQUEE KIT...
The Issue: Disposable biopsy instruments were potentially manufactured missing the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: IMMULITE 2000 PSA assay Recalled by Siemens Healthcare Diagnostics, Inc. Due...
The Issue: The IMMULITE 2000 PSA assay for use on the IMMULITE 2000 and IMMULITE 2000...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 1) Flex Extenders Recalled by Westmed, Inc. Due to Due to connector within...
The Issue: Due to connector within the circuit flex extender not meeting specifications...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Great Value Diced Peaches Recalled by Walmart Inc Due to FD&C Red No 3 was...
The Issue: FD&C Red No 3 was not declared as an ingredient.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Horizon Organic Ultra Pasteurized Heavy Whipping Cream Recalled by Horizon...
The Issue: Potential for premature product spoilage during shelf life.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Great Value Cherry Mixed Fruit Recalled by Walmart Inc Due to FD&C Red No 3...
The Issue: FD&C Red No 3 was not declared as an ingredient.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: AMBU / KING LTSD Recalled by King Systems Corp. dba Ambu, Inc. Due to Exceed...
The Issue: Exceed the limitations to the 510 (k) exemption in 21 CFR 868.9(a) because...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KING LTSD Recalled by King Systems Corp. dba Ambu, Inc. Due to Exceed the...
The Issue: Exceed the limitations to the 510 (k) exemption in 21 CFR 868.9(a) because...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KING LTSD Recalled by King Systems Corp. dba Ambu, Inc. Due to Exceed the...
The Issue: Exceed the limitations to the 510 (k) exemption in 21 CFR 868.9(a) because...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KING LTSD Recalled by King Systems Corp. dba Ambu, Inc. Due to Exceed the...
The Issue: Exceed the limitations to the 510 (k) exemption in 21 CFR 868.9(a) because...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KING LTSD Recalled by King Systems Corp. dba Ambu, Inc. Due to Exceed the...
The Issue: Exceed the limitations to the 510 (k) exemption in 21 CFR 868.9(a) because...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KING LTSD Recalled by King Systems Corp. dba Ambu, Inc. Due to Exceed the...
The Issue: Exceed the limitations to the 510 (k) exemption in 21 CFR 868.9(a) because...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KING LTSD Recalled by King Systems Corp. dba Ambu, Inc. Due to Exceed the...
The Issue: Exceed the limitations to the 510 (k) exemption in 21 CFR 868.9(a) because...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KING LTSD Recalled by King Systems Corp. dba Ambu, Inc. Due to Exceed the...
The Issue: Exceed the limitations to the 510 (k) exemption in 21 CFR 868.9(a) because...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Thiamine HCl 0.9% Sodium Chloride Injection USP Recalled by Fresenius Kabi...
The Issue: cGMP violations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Vancomycin HCl 750 mg per 250 mL 0.9% Sodium Chloride Injection USP Recalled...
The Issue: cGMP violations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: NORepinephrine Bitartrate 0.9% Sodium Chloride Injection USP Recalled by...
The Issue: cGMP violations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: NORepinephrine Bitartrate 0.9% Sodium Chloride Injection USP Recalled by...
The Issue: cGMP violations
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.