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. 1,020 recalls have been distributed to Missouri in the last 12 months.

52,570 total recalls
1,020 in last 12 months

Showing 23041–23060 of 52,570 recalls

DrugApril 25, 2019· US Worldmeds LLC

Recalled Item: Revonto (dantrolene sodium for injection) Recalled by US Worldmeds LLC Due...

The Issue: Presence of Precipitate: Appearance is Out of Specification for the...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 25, 2019· Advantice Health

Recalled Item: Dermoplast Anesthetic PAIN & ITCH (benzocaine and menthol) SPRAY canisters...

The Issue: Labeling: Not Elsewhere Classified: Full cases may contain canisters that...

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

Class III — Low RiskOngoing
Refund
DrugApril 25, 2019· Zydus Pharmaceuticals USA Inc

Recalled Item: Acyclovir Tablets Recalled by Zydus Pharmaceuticals USA Inc Due to Labeling;...

The Issue: Labeling; Label Mix-up; report received of one bottle labeled as Acyclovir...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 25, 2019· Zydus Pharmaceuticals USA Inc

Recalled Item: Carvedilol Tablets Recalled by Zydus Pharmaceuticals USA Inc Due to...

The Issue: Labeling; Label Mix-up; report received of one bottle labeled as Acyclovir...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 25, 2019· Advantice Health

Recalled Item: Dermoplast Anesthetic PAIN & ITCH (benzocaine and menthol) SPRAY canisters...

The Issue: Labeling: Not Elsewhere Classified: canisters incorrectly state the net...

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

Class III — Low RiskOngoing
Refund
DrugApril 24, 2019· MAJOR PHARMACEUTICALS

Recalled Item: DIVALPROEX SODIUM EXTENDED-RELEASE TABLETS Recalled by MAJOR PHARMACEUTICALS...

The Issue: cGMP deviations: Product was exposed above 50% relative humidity levels...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 24, 2019· AVKARE Inc.

Recalled Item: Losartan Potassium Tablets USP 50 mg 50 tablets (5x10) Unit Recalled by...

The Issue: CGMP Deviations: FDA lab confirmed presence of an impurity,...

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

Class II — Potential Health HazardOngoing
Refund
DrugApril 24, 2019· AVKARE Inc.

Recalled Item: Losartan Potassium Tablets USP 25 mg 50 tablets (5x10) Unit Recalled by...

The Issue: CGMP Deviations: FDA lab confirmed presence of an impurity,...

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

Class II — Potential Health HazardOngoing
Refund
FoodApril 24, 2019· AmeriHerb International Inc

Recalled Item: Parsley flakes Recalled by AmeriHerb International Inc Due to Potential E....

The Issue: Dried spice and herb products potentially contaminated with generic E. coli.

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

Class II — Potential Health HazardOngoing
Refund
FoodApril 24, 2019· AmeriHerb International Inc

Recalled Item: Goldenseal herb c/s Recalled by AmeriHerb International Inc Due to Potential...

The Issue: Dried spice and herb products potentially contaminated with generic E. coli.

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

Class II — Potential Health HazardOngoing
Refund
FoodApril 24, 2019· AmeriHerb International Inc

Recalled Item: Lemon balm leaf c/s Recalled by AmeriHerb International Inc Due to Potential...

The Issue: Dried spice and herb products potentially contaminated with generic E. coli.

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

Class II — Potential Health HazardOngoing
Refund
FoodApril 24, 2019· AmeriHerb International Inc

Recalled Item: Blessed thistle herb c/s Recalled by AmeriHerb International Inc Due to...

The Issue: Dried spice and herb products potentially contaminated with generic E. coli.

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

Class II — Potential Health HazardOngoing
Refund
FoodApril 24, 2019· AmeriHerb International Inc

Recalled Item: Dill weed c/s Recalled by AmeriHerb International Inc Due to Potential E....

The Issue: Dried spice and herb products potentially contaminated with generic E. coli.

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

Class II — Potential Health HazardOngoing
Refund
FoodApril 24, 2019· AmeriHerb International Inc

Recalled Item: Mullein leaf c/s Recalled by AmeriHerb International Inc Due to Potential E....

The Issue: Dried spice and herb products potentially contaminated with generic E. coli.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceApril 24, 2019· Centurion Medical Products Corporation

Recalled Item: PICC Line Accessory Kit CVI4285 Recalled by Centurion Medical Products...

The Issue: Firm distributes kits which include the BD MaxZeroNeedleess Connector, which...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 24, 2019· Centurion Medical Products Corporation

Recalled Item: CENTRAL LINE BUNDLE 16CM MULTIMED ECVC6545A Recalled by Centurion Medical...

The Issue: Firm distributes kits which include the BD MaxZeroNeedleess Connector, which...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 24, 2019· Centurion Medical Products Corporation

Recalled Item: INVASIVE PROCEDURE TRAY MNS9510 Recalled by Centurion Medical Products...

The Issue: Firm distributes kits which include the BD MaxZeroNeedleess Connector, which...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 24, 2019· Centurion Medical Products Corporation

Recalled Item: CVC BUNDLE Recalled by Centurion Medical Products Corporation Due to Firm...

The Issue: Firm distributes kits which include the BD MaxZeroNeedleess Connector, which...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 24, 2019· Centurion Medical Products Corporation

Recalled Item: TRIPLE LUMEN CVC 20CM BUNDLE STCVC2040 Recalled by Centurion Medical...

The Issue: Firm distributes kits which include the BD MaxZeroNeedleess Connector, which...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 24, 2019· Centurion Medical Products Corporation

Recalled Item: CVC BUNDLE VANTEX 7F Recalled by Centurion Medical Products Corporation Due...

The Issue: Firm distributes kits which include the BD MaxZeroNeedleess Connector, which...

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

Class II — Potential Health HazardOngoing