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.
Showing 26381–26400 of 29,298 recalls
Recalled Item: Brilliance CT Big Bore Oncology Recalled by Philips Medical Systems...
The Issue: There are artifacts appearing on the Tracker images during...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SmartSite Low Sorbing Infusion Set Recalled by CareFusion 303, Inc. Due to...
The Issue: CareFusion is recalling the SmartSite Low Sorbing Infusion Set, Model#...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Emit 2000 Phenobarbital Assay and Syva Emit 2000 Phenobarbital Assay...
The Issue: Imprecision with certain lots
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sidus" Head (Not distributed in the United States) Recalled by Zimmer, Inc....
The Issue: The low density polyethylene (LDPE) bag used to package implants adheres to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Multipolar¿ Bipolar Cup METAL SHELL 38 MM OD through 71 Recalled by Zimmer,...
The Issue: The low density polyethylene (LDPE) bag used to package implants adheres to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CPT¿ Femoral Stem (CPT 12/14 STEM SIZE 0 COCR Recalled by Zimmer, Inc. Due...
The Issue: The low density polyethylene (LDPE) bag used to package implants adheres to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Natural-Knee¿ Flex Femoral Component. Provides increased flexion capability....
The Issue: The low density polyethylene (LDPE) bag used to package implants adheres to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CoCr Head (Not distributed in the United States) Used in Recalled by Zimmer,...
The Issue: The low density polyethylene (LDPE) bag used to package implants adheres to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Metasul¿ Head. Intended for use either with or without bone Recalled by...
The Issue: The low density polyethylene (LDPE) bag used to package implants adheres to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NexGen¿ Femoral Component (CR-FLEX GSF POR FEM Recalled by Zimmer, Inc. Due...
The Issue: The low density polyethylene (LDPE) bag used to package implants adheres to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vented Spike Adapter Product Code 2C0471 Recalled by Baxter Healthcare Corp....
The Issue: Potential tears in the pouch of six lots of Vented Spike Adapter Product...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Device Name: Terino Square Chin-Style II-Medium Recalled by Implantech...
The Issue: Implantech initiated a voluntary recall of certain lots of Terino Square...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Recalled by GE Healthcare, LLC Due to GE Healthcare has...
The Issue: GE Healthcare has recently become aware of a potential safety issue...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Gender Solutions" Patello-Femoral Component Recalled by Zimmer, Inc. Due to...
The Issue: The low density polyethylene (LDPE) bag used to package implants adheres to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NexGen¿ Femoral Component (CR-FLEX GSF PRECOAT SZ C-L Recalled by Zimmer,...
The Issue: The low density polyethylene (LDPE) bag used to package implants adheres to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Boston Scientific COGNIS CRT-D Recalled by Boston Scientific CRM Corp Due to...
The Issue: The performance of a low voltage capacitor in a subset of COGNIS CRT-Ds and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CARESTREAM DRX -Mobile Retrofit Kit Recalled by Carestream Health Inc. Due...
The Issue: Carestream Health Inc. has conducted a voluntary field action which includes...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Vital Diagnostics Envoy Calcium Reagent For In-Vitro Diagnostic Use. PN...
The Issue: High positive calcium bias on plasma sample versus results on serum
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 2008K@ Home Blood lines Combiset True Flow Series for Hemodialysis Recalled...
The Issue: Updated Instructions for Use: Bloodline connections not tightened per...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: DRX- Revolution Recalled by Carestream Health Inc. Due to Carestream Health...
The Issue: Carestream Health Inc. has conducted a voluntary field action which includes...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.