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. 1,894 recalls have been distributed to Missouri in the last 12 months.

52,570 total recalls
1,894 in last 12 months

Showing 2864128660 of 52,570 recalls

DrugOctober 19, 2017· SCA Pharmaceuticals, LLC

Recalled Item: morphine sulfate 1 mg per mL in 0.9% Sodium Chloride Recalled by SCA...

The Issue: Lack Of Assurance Of Sterility.

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 19, 2017· SCA Pharmaceuticals, LLC

Recalled Item: SUCcinylcholine 20 mg per mL Recalled by SCA Pharmaceuticals, LLC Due to...

The Issue: Lack Of Assurance Of Sterility.

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 19, 2017· SCA Pharmaceuticals, LLC

Recalled Item: PHENYLephrine HCl 100 mcg per mL In 0.9% Sodium Chloride Recalled by SCA...

The Issue: Lack Of Assurance Of Sterility.

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 19, 2017· SCA Pharmaceuticals, LLC

Recalled Item: Calcium GLUCOnate 2 g added to 0.9% Sodium Chloride 50 mL Bag Recalled by...

The Issue: Lack Of Assurance Of Sterility.

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

Class II — Potential Health HazardOngoing
Refund
DrugOctober 19, 2017· SCA Pharmaceuticals, LLC

Recalled Item: HYDROmorphone HCl 20 mcg / mL BUPIvacaine HCl 0.075% in Recalled by SCA...

The Issue: Lack Of Assurance Of Sterility.

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

Class II — Potential Health HazardOngoing
Refund
Medical DeviceOctober 19, 2017· Datascope Corporation

Recalled Item: BEQ-TOP 41201 ECC 3/8 PUMP PAC Recalled by Datascope Corporation Due to The...

The Issue: The Better Bladder device provided as part of some custom tubing kits has...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 19, 2017· Datascope Corporation

Recalled Item: BEQ-TOP 24500 ADULT ECC Recalled by Datascope Corporation Due to The Better...

The Issue: The Better Bladder device provided as part of some custom tubing kits has...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 19, 2017· Datascope Corporation

Recalled Item: BEQ-T 9410 Lurie Chldns Small 1/4 Recalled by Datascope Corporation Due to...

The Issue: The Better Bladder device provided as part of some custom tubing kits has...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 19, 2017· Johnson & Johnson Vision Care, Inc.

Recalled Item: ACUVUE OASYS Brand Contact Lenses with HYDRACLEAR PLUS Recalled by Johnson &...

The Issue: Some contact lenses were associated with complaints of a foreign matter...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 19, 2017· Johnson & Johnson Vision Care, Inc.

Recalled Item: 1-DAY ACUVUE Moist for ASTIGMATISM Brand Contact Lenses Recalled by Johnson...

The Issue: Some contact lenses were associated with complaints of a foreign matter...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 19, 2017· Datascope Corporation

Recalled Item: BEQ-TOP 22701 Recalled by Datascope Corporation Due to The Better Bladder...

The Issue: The Better Bladder device provided as part of some custom tubing kits has...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 19, 2017· Cook Inc.

Recalled Item: Wills-Oglesby Percutaneous Gastrostomy Set Product Usage: Intended for the...

The Issue: Cook has identified that the affected lots may contain wire guides that were...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 19, 2017· Datascope Corporation

Recalled Item: BEQ-T 25501 3/8" Better Bladder Pack Recalled by Datascope Corporation Due...

The Issue: The Better Bladder device provided as part of some custom tubing kits has...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 19, 2017· Datascope Corporation

Recalled Item: BEQ-TOP 40700 HUNTINGTON Recalled by Datascope Corporation Due to The Better...

The Issue: The Better Bladder device provided as part of some custom tubing kits has...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 19, 2017· Datascope Corporation

Recalled Item: ECC Small - Respiratory BEQ-TOP 5210 Recalled by Datascope Corporation Due...

The Issue: The Better Bladder device provided as part of some custom tubing kits has...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 19, 2017· Datascope Corporation

Recalled Item: BO-TOP 20700 SMALL PATIENT 3/8 Recalled by Datascope Corporation Due to The...

The Issue: The Better Bladder device provided as part of some custom tubing kits has...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 19, 2017· Datascope Corporation

Recalled Item: BO-TOP 13901 RAPID RESPONSE Recalled by Datascope Corporation Due to The...

The Issue: The Better Bladder device provided as part of some custom tubing kits has...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 19, 2017· Datascope Corporation

Recalled Item: BEQ-TOP 8504 1/4X1/4 PACK W/QP Recalled by Datascope Corporation Due to The...

The Issue: The Better Bladder device provided as part of some custom tubing kits has...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 19, 2017· Datascope Corporation

Recalled Item: Adult ECC Pack BEQ-TOP 22300 Recalled by Datascope Corporation Due to The...

The Issue: The Better Bladder device provided as part of some custom tubing kits has...

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

Class II — Potential Health HazardOngoing
Medical DeviceOctober 19, 2017· Datascope Corporation

Recalled Item: BEQ-TOP 5210 ECC Set - Respiratory Recalled by Datascope Corporation Due to...

The Issue: The Better Bladder device provided as part of some custom tubing kits has...

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

Class II — Potential Health HazardOngoing