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. 1,870 recalls have been distributed to Missouri in the last 12 months.

52,570 total recalls
1,870 in last 12 months

Showing 3144131460 of 52,570 recalls

FoodMarch 27, 2017· Givaudan Flavours Corp

Recalled Item: SJ DRY BROWNIE MIX 1003706 Net Wgt: 1200 LBS INGREDIENTS: Sugar Recalled by...

The Issue: During an internal investigation the firm discovered that an ingredient used...

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

Class II — Potential Health HazardOngoing
Refund
FoodMarch 27, 2017· Givaudan Flavours Corp

Recalled Item: SJ JALAPENO NACHO DB 42 LBS INGREDIENTS: Dextrose Recalled by Givaudan...

The Issue: During an internal investigation the firm discovered that an ingredient used...

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

Class II — Potential Health HazardOngoing
Refund
FoodMarch 27, 2017· Givaudan Flavours Corp

Recalled Item: SJ PHILLY CHEESESTEAK SEASONING Net Wt: .44.5 LBS INGREDIENTS: Onion Powder...

The Issue: During an internal investigation the firm discovered that an ingredient used...

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

Class II — Potential Health HazardOngoing
Refund
FoodMarch 27, 2017· Givaudan Flavours Corp

Recalled Item: SJ TABASCO Net Wgt: 36.33 LBS INGREDIENTS: Spices including Mustard Recalled...

The Issue: During an internal investigation the firm discovered that an ingredient used...

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

Class II — Potential Health HazardOngoing
Refund
FoodMarch 27, 2017· Givaudan Flavours Corp

Recalled Item: SJ SWEET AND SPICY Net Wt: 42.75 LBS INGREDIENTS: Brown Sugar Recalled by...

The Issue: During an internal investigation the firm discovered that an ingredient used...

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

Class II — Potential Health HazardOngoing
Refund
FoodMarch 27, 2017· Givaudan Flavours Corp

Recalled Item: Chili Seasoning 50 lbs INGREDIENTS: Chili Pepper Recalled by Givaudan...

The Issue: During an internal investigation the firm discovered that an ingredient used...

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

Class II — Potential Health HazardOngoing
Refund
FoodMarch 27, 2017· Givaudan Flavours Corp

Recalled Item: SJ CHIPOLTE BBQ DB 36.7 lbs INGREDIENTS: SALT Recalled by Givaudan Flavours...

The Issue: During an internal investigation the firm discovered that an ingredient used...

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

Class II — Potential Health HazardOngoing
Refund
FoodMarch 27, 2017· Givaudan Flavours Corp

Recalled Item: SJ Black Pepper 42.75 lbs INGREDIENTS: Black Pepper Recalled by Givaudan...

The Issue: During an internal investigation the firm discovered that an ingredient used...

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

Class II — Potential Health HazardOngoing
Refund
FoodMarch 27, 2017· Givaudan Flavours Corp

Recalled Item: SJ SPICY DB Net Wt. 48 LBS INGREDIENTS: Spices including Mustard Recalled by...

The Issue: During an internal investigation the firm discovered that an ingredient used...

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceMarch 27, 2017· Alcon Research, Ltd.

Recalled Item: Alcon Patient Care Kits Product Usage: A Patient Care Kit Recalled by Alcon...

The Issue: Alcon is initiating a Voluntary Medical Device Removal because the product...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 24, 2017· Craftmatic Industries, Inc.

Recalled Item: Craftmatic Model 1 Base for Dual Bed Configurations Recalled by Craftmatic...

The Issue: A potential for dual-configured beds to separate or slip away from one another.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 24, 2017· Craftmatic Industries, Inc.

Recalled Item: Legacy Base for Dual Bed Configurations Recalled by Craftmatic Industries,...

The Issue: A potential for dual-configured beds to separate or slip away from one another.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 24, 2017· Arthrex, Inc.

Recalled Item: Anthrex Bio-SwiveLock SP Vented Recalled by Arthrex, Inc. Due to Some...

The Issue: Some eyelets broke from SwiveLock Anchor on insertion.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 24, 2017· Arthrex, Inc.

Recalled Item: Anthrex SpeedBridge Implant System with BioComposite SwiveLock SP Vented...

The Issue: Some eyelets broke from SwiveLock Anchor on insertion.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 24, 2017· Arthrex, Inc.

Recalled Item: Anthrex PEEK SwiveLock SP Vented Recalled by Arthrex, Inc. Due to Some...

The Issue: Some eyelets broke from SwiveLock Anchor on insertion.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 24, 2017· Arthrex, Inc.

Recalled Item: Anthrex PEEK SwiveLock SP Vented Recalled by Arthrex, Inc. Due to Some...

The Issue: Some eyelets broke from SwiveLock Anchor on insertion.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 24, 2017· Arthrex, Inc.

Recalled Item: Anthrex Bio Composite SwiveLock SP Vented Recalled by Arthrex, Inc. Due to...

The Issue: Some eyelets broke from SwiveLock Anchor on insertion.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 24, 2017· Arthrex, Inc.

Recalled Item: Anthrex SpeedBridge Implant System with PEEK SwiveLock Self Punching...

The Issue: Some eyelets broke from SwiveLock Anchor on insertion.

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 24, 2017· Dale Medical Products, Inc.

Recalled Item: Dale Medical Stabilock Endotracheal Adhesive Base Product # 273 The Recalled...

The Issue: ET Tube Holders contain an adhesive faceplate that may lose its adhesive...

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

Class II — Potential Health HazardOngoing
Medical DeviceMarch 24, 2017· Dale Medical Products, Inc.

Recalled Item: Dale Medical Stabilock Endotracheal Tube Holder Product # 270 The Recalled...

The Issue: ET Tube Holders contain an adhesive faceplate that may lose its adhesive...

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

Class II — Potential Health HazardOngoing