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. 1,060 recalls have been distributed to Missouri in the last 12 months.

52,570 total recalls
1,060 in last 12 months

Showing 14601–14620 of 52,570 recalls

FoodOctober 28, 2021· MARY RUTH ORGANICS

Recalled Item: MaryRuth's Organic Infants Liquid Probiotic Recalled by MARY RUTH ORGANICS...

The Issue: Internal testing found the presence of Pseudomonas aeruginosa in the product.

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceOctober 28, 2021· Palodex Group Oy

Recalled Item: Orthopantomograph OP300 dental computed tomography x-ray system. The X-ray...

The Issue: It was noticed in production on 28.10.2021, that the final testing database...

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

Class II — Potential Health HazardOngoing
DrugOctober 28, 2021· Teva Pharmaceuticals USA

Recalled Item: Clonidine Transdermal System Recalled by Teva Pharmaceuticals USA Due to...

The Issue: Failed Impurities/Degradation Specifications

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

Class III — Low RiskOngoing
Refund
DrugOctober 28, 2021· Apollo Care

Recalled Item: VANComycin 1g added to 250mL of 0.9% Sodium Chloride (Injection Recalled by...

The Issue: Crystallization: Product appears to be turbid.

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 27, 2021· Teva Pharmaceuticals USA

Recalled Item: Cartia XT (Diltiazem Hydrochloride Extended-Release Capsules Recalled by...

The Issue: Labelling: Incorrect Exp. Date

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceOctober 27, 2021· Medline Industries Inc

Recalled Item: Bedside PICC CDS Convenience Kit Recalled by Medline Industries Inc Due to...

The Issue: NaCl 250 mL Bag Inj expired 04/2020 while the kit expiration date was after...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 27, 2021· Medline Industries Inc

Recalled Item: Venous Access Pack-LF Convenience Kit Recalled by Medline Industries Inc Due...

The Issue: NaCl 250 mL Bag Inj expired 04/2020 while the kit expiration date was after...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 27, 2021· Medline Industries Inc

Recalled Item: Neuro Convenience Kit Recalled by Medline Industries Inc Due to NaCl 250 mL...

The Issue: NaCl 250 mL Bag Inj expired 04/2020 while the kit expiration date was after...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 27, 2021· Medline Industries Inc

Recalled Item: Major Vascular CDS Convenience Kit Recalled by Medline Industries Inc Due to...

The Issue: NaCl 250 mL Bag Inj expired 04/2020 while the kit expiration date was after...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 27, 2021· Medline Industries Inc

Recalled Item: EVLP Convenience Pack/Kit Recalled by Medline Industries Inc Due to NaCl 250...

The Issue: NaCl 250 mL Bag Inj expired 04/2020 while the kit expiration date was after...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 26, 2021· MAX LUX CORP

Recalled Item: The product is a handheld ultraviolet-C germicidal wand and contains two...

The Issue: Excessive ultraviolet-C radiation

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

Class II — Potential Health HazardOngoing
DrugOctober 26, 2021· Perrigo Company PLC

Recalled Item: Acetaminophen Child Dye Free Cherry Flavor Oral Suspension (160mg/5ml)...

The Issue: CGMP Deviations: Products were manufactured with contaminated excipient that...

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 26, 2021· Perrigo Company PLC

Recalled Item: Sinus Severe Recalled by Perrigo Company PLC Due to CGMP Deviations:...

The Issue: CGMP Deviations: Products were manufactured with contaminated excipient that...

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 26, 2021· Perrigo Company PLC

Recalled Item: Maximum Strength No Drip Nasal Spray Recalled by Perrigo Company PLC Due to...

The Issue: CGMP Deviations: Products were manufactured with contaminated excipient that...

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 26, 2021· Perrigo Company PLC

Recalled Item: Children's Grape Flavored Acetaminophen Oral Suspension (160mg/5ml) Recalled...

The Issue: CGMP Deviations: Products were manufactured with contaminated excipient that...

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 26, 2021· Perrigo Company PLC

Recalled Item: Acetaminophen Child Dye Free Cherry Flavor Oral Suspension (160mg/5ml)...

The Issue: CGMP Deviations: Products were manufactured with contaminated excipient that...

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 26, 2021· Perrigo Company PLC

Recalled Item: No Drip Nasal Decongestant Recalled by Perrigo Company PLC Due to CGMP...

The Issue: CGMP Deviations: Products were manufactured with contaminated excipient that...

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 26, 2021· Perrigo Company PLC

Recalled Item: Infant's Grape Flavored Acetaminophen Oral Suspension (160mg/5ml) Recalled...

The Issue: CGMP Deviations: Products were manufactured with contaminated excipient that...

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 26, 2021· Perrigo Company PLC

Recalled Item: Maxiumum Strength No Drip Nasal Spray Recalled by Perrigo Company PLC Due to...

The Issue: CGMP Deviations: Products were manufactured with contaminated excipient that...

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 26, 2021· Perrigo Company PLC

Recalled Item: Acetaminophen Infant Dye Free Grape Oral Suspension (160mg/5ml) Recalled by...

The Issue: CGMP Deviations: Products were manufactured with contaminated excipient that...

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

Class II — Potential Health HazardOngoing
Refund