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. 970 recalls have been distributed to Missouri in the last 12 months.
Showing 38461–38480 of 52,570 recalls
Recalled Item: Ferno iNX Wheeled Stretcher Recalled by Ferno-Washington Inc Due to Hole...
The Issue: Hole elongation in the telescoping load frame channel. A hole elongation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Rivastigmine Tartrate Capsules Recalled by Dr. Reddy's Laboratories, Inc....
The Issue: Failed Dissolution Specifications
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Edwards Pressure Monitoring Kit with TruWave disposable pressure transducer....
The Issue: Flow restriction issues in a trifurcated IV set included in the pressure...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Voyant Open Fusion Device Models: EB040 and EB040+ Product Usage: Recalled...
The Issue: Potential to improperly characterize tissue within the jaws, which may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Covidien Argyle Infant Heel Warmers (with tab) Item Code: MH00002T Recalled...
The Issue: Infant Heel warmers may break during activation resulting in spillage of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 2.4 Recalled by Trilliant Surgical Ltd. Due to Gridlock screw driver bits...
The Issue: Gridlock screw driver bits for the Gridlock Plating System were identified...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Covidien Argyle Infant Heel Warmers (no tab) Item Code: MH00002N Recalled by...
The Issue: Infant Heel warmers may break during activation resulting in spillage of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens Symbia T Series Recalled by Siemens Medical Solutions USA, Inc. Due...
The Issue: Fuses with the improper amperage rating were installed in the Symbia S,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AngioJet SOLENT Dista Thrombectomy Set: UPN 111303-001 Recalled by Boston...
The Issue: AngioJet products were distributed with an incorrect use-by (expiry) date....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AngioJet SOLENT Omni Thrombectomy Set: UPN 109681-004 & 109681-001 Recalled...
The Issue: AngioJet products were distributed with an incorrect use-by (expiry) date....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AngioJet AVX Thrombectomy Set: UPN 105039-001 Recalled by Boston Scientific...
The Issue: AngioJet products were distributed with an incorrect use-by (expiry) date....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AngioJet Spiroflex Thrombectomy Set: Peripheral - UPN 106553-004 Recalled by...
The Issue: AngioJet products were distributed with an incorrect use-by (expiry) date....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens Symbia S Series system Recalled by Siemens Medical Solutions USA,...
The Issue: Fuses with the improper amperage rating were installed in the Symbia S,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Siemens Intevo Series system Recalled by Siemens Medical Solutions USA, Inc....
The Issue: Fuses with the improper amperage rating were installed in the Symbia S,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PICC Kits with Peel-Away Sheath Component Recalled by Arrow International...
The Issue: the catheter peel-away component hub tabs may prematurely detach. One injury...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AU5800 Chemistry Analyzers Recalled by Beckman Coulter Inc. Due to Beckman...
The Issue: Beckman coulter has received complaints regarding leaking and cracked C...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AU680 Chemistry Analyzers Recalled by Beckman Coulter Inc. Due to Beckman...
The Issue: Beckman coulter has received complaints regarding leaking and cracked C...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AU480 Chemistry Analyzers Recalled by Beckman Coulter Inc. Due to Beckman...
The Issue: Beckman coulter has received complaints regarding leaking and cracked C...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arrow International Recalled by Arrow International Inc Due to saline...
The Issue: saline leakage from unsecured connections between the Touhy Borst adaptor...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: JBN (Just Be Natural) Growtein Growth Protein Chocolate NET WT. Recalled by...
The Issue: Protein powders and nutritional supplement products made of whey...
Recommended Action: Do not consume. Return to store for a refund or discard.