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. 1,747 recalls have been distributed to Missouri in the last 12 months.
Showing 49701–49720 of 52,570 recalls
Recalled Item: Merit Medical Systems Inc. Recalled by Merit Medical Systems, Inc. Due to A...
The Issue: A consumer complaint that a catheter was observed to be in several pieces...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Diagnost Stationary Radiographic System Models: 712020 Recalled by...
The Issue: Installation Acceptance Test Document (IATD) non compliant with regulations....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Carvedilol Tablets Recalled by Mylan Pharmaceuticals Inc. Due to Failed...
The Issue: Failed Tablet/Capsule Specifications: Product exceeds specification for...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: DePuy CONFIDENCE SPINAL CEMENT SYSTEM 5CC KIT Catalog Number:283905000....
The Issue: Cement mixer used to prepare cement for surgery may not turn properly and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Spacelabs BleaseSirius Anesthesia Workstation Recalled by Del Mar Reynolds...
The Issue: A defect in CAS I/II Absorbers in the Spacelabs Anesthesia Workstations and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DePuy CONFIDENCE SPINAL CEMENT SYSTEM KIT Catalog Number: 283913000....
The Issue: Cement mixer used to prepare cement for surgery may not turn properly and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DePuy CONFIDENCE SPINAL CEMENT SYSTEM 11C Plus KIT Catalog Number: Recalled...
The Issue: Cement mixer used to prepare cement for surgery may not turn properly and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Iconos R200 C20 Recalled by Siemens Medical Solutions USA, Inc Due to...
The Issue: Siemens has become aware of a potential malfunction and possible hazard to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DePuy CONFIDENCE SPINAL CEMENT SYSTEM 7CC KIT Catalog Number: 283907000....
The Issue: Cement mixer used to prepare cement for surgery may not turn properly and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BREG Cold Therapy Combination Units containing Sterile Polar Pads. 02356 Rev...
The Issue: The recall was initiated because Breg has determined that some Sterile Polar...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Atricure Inc. Recalled by Atricure Inc Due to Products from lot no. 41865...
The Issue: Products from lot no. 41865 may have been sent out with Incorrect...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Senographe Essential System. The Senographe 2000D system...
The Issue: GE Healthcare has recently become aware of a potential issue due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BREG Sterile Polar Pads Recalled by Breg Inc Due to The recall was initiated...
The Issue: The recall was initiated because Breg has determined that some Sterile Polar...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LifeStyles ZERO 10 uber-thin lubricated latex condoms. Mfd. for Ansell...
The Issue: Out of an abundance of caution, Ansell is implementing a voluntary recall of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips Healthcare SureSigns VS2+ Model 863278 SureSigns VS2+ NBP and...
The Issue: VS2+ screen may lock up and stop monitoring during patient use
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: P10 Tobii battery box (product number 510410) Product Usage - Recalled by...
The Issue: Tobii ATI customers P10 external battery pack, which contains sealed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Inspira AIR Balloon Dilation system. Size 10 x 40 mm Recalled by Acclarent,...
The Issue: Labeling correction for all sizes of the Inspira AIR Balloon Dilation System...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NEUROPATH 6Fx100 GUIDING CATH MP Product Code: GMD61000000 Intended for...
The Issue: Sterility of device may be compromised due to lack of package integrity
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NEUROPATH 6Fx100 GUIDING CATH ST Product Code: GST61000000 Intended for...
The Issue: Sterility of device may be compromised due to lack of package integrity
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NEUROPATH 6Fx100 GUIDING CATH S2 Product Code: GSM61000000 Intended for...
The Issue: Sterility of device may be compromised due to lack of package integrity
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.