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. 1,827 recalls have been distributed to Missouri in the last 12 months.

52,570 total recalls
1,827 in last 12 months

Showing 3542135440 of 52,570 recalls

Medical DeviceApril 22, 2016· Siemens Medical Solutions USA Inc.

Recalled Item: BIOGRAPH 6 TruePoint Recalled by Siemens Medical Solutions USA Inc. Due to...

The Issue: Siemens Medical Solutions, Molecular Imaging has become aware of a potential...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 22, 2016· Siemens Medical Solutions USA Inc.

Recalled Item: BIOGRAPH mCT Flow Edge-4R Recalled by Siemens Medical Solutions USA Inc. Due...

The Issue: Siemens Medical Solutions, Molecular Imaging has become aware of a potential...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 22, 2016· Siemens Medical Solutions USA Inc.

Recalled Item: BIOGRAPH mCT S(20) - 3R Recalled by Siemens Medical Solutions USA Inc. Due...

The Issue: Siemens Medical Solutions, Molecular Imaging has become aware of a potential...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 22, 2016· Siemens Medical Solutions USA Inc.

Recalled Item: BIOGRAPH mCT Flow 20-3R Recalled by Siemens Medical Solutions USA Inc. Due...

The Issue: Siemens Medical Solutions, Molecular Imaging has become aware of a potential...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 22, 2016· Siemens Medical Solutions USA Inc.

Recalled Item: BIOGRAPH mCT Flow 40-4R Recalled by Siemens Medical Solutions USA Inc. Due...

The Issue: Siemens Medical Solutions, Molecular Imaging has become aware of a potential...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 22, 2016· Siemens Medical Solutions USA Inc.

Recalled Item: BIOGRAPH mCT Flow Edge-3R Recalled by Siemens Medical Solutions USA Inc. Due...

The Issue: Siemens Medical Solutions, Molecular Imaging has become aware of a potential...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 22, 2016· Siemens Medical Solutions USA Inc.

Recalled Item: Biograph 16 TruePoint TV Recalled by Siemens Medical Solutions USA Inc. Due...

The Issue: Siemens Medical Solutions, Molecular Imaging has become aware of a potential...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 22, 2016· Siemens Medical Solutions USA Inc.

Recalled Item: BIOGRAPH 40 - 3 Ring Recalled by Siemens Medical Solutions USA Inc. Due to...

The Issue: Siemens Medical Solutions, Molecular Imaging has become aware of a potential...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 22, 2016· Siemens Medical Solutions USA Inc.

Recalled Item: BIOGRAPH 40 TruePoint Recalled by Siemens Medical Solutions USA Inc. Due to...

The Issue: Siemens Medical Solutions, Molecular Imaging has become aware of a potential...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 22, 2016· RTI Surgical, Inc. (dba Pioneer Surgical Technology, Inc.)

Recalled Item: Streamline OCT Occipito-Cervico-Thoracic System Recalled by RTI Surgical,...

The Issue: Potential for a product defect where the cannula may be obstructed. This...

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

Class II — Potential Health HazardOngoing
FoodApril 21, 2016· Vitalicious Acquisition

Recalled Item: VitaTops Apple Crumb Recalled by Vitalicious Acquisition Due to Undeclared Milk

The Issue: The affected lots of VitaTops Apple Crumb contain undeclared milk.

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

Class I — Serious Health HazardOngoing
Refund
FoodApril 21, 2016· 7-Eleven, Inc.

Recalled Item: Oatmeal Raisin Cookies prepared in store and sold in bakery Recalled by...

The Issue: Undeclared peanuts in fully-baked cookies.

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

Class I — Serious Health HazardOngoing
Refund
FoodApril 21, 2016· 7-Eleven, Inc.

Recalled Item: Sugar Cookies prepared in store and sold in bakery cases for self-service....

The Issue: Undeclared peanuts in fully-baked cookies.

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

Class I — Serious Health HazardOngoing
Refund
FoodApril 21, 2016· 7-Eleven, Inc.

Recalled Item: Chocolate Chunk Cookies prepared in store and sold in bakery Recalled by...

The Issue: Undeclared peanuts in fully-baked cookies.

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

Class I — Serious Health HazardOngoing
Refund
Medical DeviceApril 21, 2016· Musculoskeletal Transplant Foundation, Inc.

Recalled Item: Musculoskeletal Transplant Foundation Recalled by Musculoskeletal Transplant...

The Issue: AFT Diverted Tubes are being recalled due to a customer complaint involving...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 21, 2016· Miami Fat Supply, Inc

Recalled Item: The Red Head 2 Reusable Fat Harvesting Canister Recalled by Miami Fat...

The Issue: During an FDA inspection it was found that the products are marketed without...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 21, 2016· Draeger Medical, Inc.

Recalled Item: Draeger D-Vapor/ D-Vapor 3000 Vaporizers with Baxter Desflurane Agent and...

The Issue: Operators noticed unwanted release of evaporating anesthetic agent at the...

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 21, 2016· Baxter Healthcare Corp.

Recalled Item: GEM(TM) Recalled by Baxter Healthcare Corp. Due to Instructions for use...

The Issue: Instructions for use booklet may puncture the outer Tyvek lid.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 21, 2016· Baxter Healthcare Corp.

Recalled Item: GEM(TM) Recalled by Baxter Healthcare Corp. Due to Instructions for use...

The Issue: Instructions for use booklet may puncture the outer Tyvek lid.

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

Class II — Potential Health HazardOngoing
Medical DeviceApril 21, 2016· Baxter Healthcare Corp.

Recalled Item: GEM(TM) Recalled by Baxter Healthcare Corp. Due to Instructions for use...

The Issue: Instructions for use booklet may puncture the outer Tyvek lid.

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

Class II — Potential Health HazardOngoing