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. 1,002 recalls have been distributed to Missouri in the last 12 months.

52,570 total recalls
1,002 in last 12 months

Showing 30161–30180 of 52,570 recalls

FoodJune 8, 2017· National Fish & Seafood, Inc.

Recalled Item: FALCON BAIE BRAND PRECOOKED FISH PORTIONS MADE FROM MINCED FISH Recalled by...

The Issue: Product may contain undeclared milk.

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

Class II — Potential Health HazardOngoing
Refund
FoodJune 8, 2017· National Fish & Seafood, Inc.

Recalled Item: LIL FISHERMAN PRE COOKED POLLOCK NUGGETS 1 OZ PUFI 1/10 LB Recalled by...

The Issue: Product may contain undeclared milk.

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

Class II — Potential Health HazardOngoing
Refund
FoodJune 8, 2017· National Fish & Seafood, Inc.

Recalled Item: NORTHSIDE PRE COOKED FLOUNDER FILLETS 4 OZ 1/10 LB Recalled by National Fish...

The Issue: Product may contain undeclared milk.

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

Class II — Potential Health HazardOngoing
Refund
FoodJune 8, 2017· National Fish & Seafood, Inc.

Recalled Item: SCHOONER PRE COOKED CRUNCHY FISH PORTIONS 12/16 OZ Recalled by National Fish...

The Issue: Product may contain undeclared milk.

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

Class II — Potential Health HazardOngoing
Refund
FoodJune 8, 2017· National Fish & Seafood, Inc.

Recalled Item: SCHOONER PRE-COOKED CRUNCHY FLOUNDER FILLETS 12/16 OZ Recalled by National...

The Issue: Product may contain undeclared milk.

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

Class II — Potential Health HazardOngoing
Refund
FoodJune 8, 2017· National Fish & Seafood, Inc.

Recalled Item: 365 EVERYDAY VALUE ALL NATURAL PRECOOKED BREADED FISH STICKS 10/2 Recalled...

The Issue: Product may contain undeclared milk.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJune 7, 2017· Terumo Medical Corp

Recalled Item: Glidesheath Slender Hydrophilic Coated Introducer Sheath Recalled by Terumo...

The Issue: An incomplete seal at the chevron end of the primary packaging of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 7, 2017· Cenorin, LLC

Recalled Item: ThermaSure(TM) Recalled by Cenorin, LLC Due to Dryer unit not heating....

The Issue: Dryer unit not heating. Manufacturing issue causes the terminal block to...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 7, 2017· Philips Medical Systems (Cleveland) Inc

Recalled Item: Brilliance iCT SP (Model No. 728311 Recalled by Philips Medical Systems...

The Issue: It was reported that scanners running certain software versions provide...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 7, 2017· Terumo Medical Corp

Recalled Item: Glidesheath Slender Hydrophilic Coated Introducer Sheath Recalled by Terumo...

The Issue: An incomplete seal at the chevron end of the primary packaging of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 7, 2017· Terumo Medical Corp

Recalled Item: Glidesheath Slender Hydrophilic Coated Introducer Sheath A-Kit Recalled by...

The Issue: An incomplete seal at the chevron end of the primary packaging of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 7, 2017· Terumo Medical Corp

Recalled Item: Glidesheath Slender Hydrophilic Coated Introducer Sheath Recalled by Terumo...

The Issue: An incomplete seal at the chevron end of the primary packaging of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 7, 2017· Philips Medical Systems (Cleveland) Inc

Recalled Item: Brilliance iCT (Model No. 728306) Recalled by Philips Medical Systems...

The Issue: It was reported that scanners running certain software versions provide...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 7, 2017· Mako Surgical Corporation

Recalled Item: MAKO RIO Standard System Recalled by Mako Surgical Corporation Due to An...

The Issue: An intermittent electrical problem that could lead to a loss of system power...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 7, 2017· Cenorin, LLC

Recalled Item: ThermaSure(TM) Recalled by Cenorin, LLC Due to Dryer unit not heating....

The Issue: Dryer unit not heating. Manufacturing issue causes the terminal block to...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 7, 2017· Terumo Medical Corp

Recalled Item: Glidesheath Slender Hydrophilic Coated Introducer Sheath Recalled by Terumo...

The Issue: An incomplete seal at the chevron end of the primary packaging of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 7, 2017· Terumo Medical Corp

Recalled Item: Glidesheath Slender Hydrophilic Coated Introducer Sheath Recalled by Terumo...

The Issue: An incomplete seal at the chevron end of the primary packaging of the...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 7, 2017· Philips Medical Systems (Cleveland) Inc

Recalled Item: IQon Spectral CT (Model No. 728332) Recalled by Philips Medical Systems...

The Issue: It was reported that scanners running certain software versions provide...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 7, 2017· DeRoyal Industries Inc

Recalled Item: DeRoyal(R) Dolphin Inflation Device Recalled by DeRoyal Industries Inc Due...

The Issue: Lack of sterility assurance. There is a defect in the primary packaging of...

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

Class II — Potential Health HazardOngoing
Medical DeviceJune 7, 2017· Terumo Medical Corp

Recalled Item: Glidesheath Slender Hydrophilic Coated Introducer Sheath Recalled by Terumo...

The Issue: An incomplete seal at the chevron end of the primary packaging of the...

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

Class II — Potential Health HazardOngoing