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. 1,918 recalls have been distributed to Missouri in the last 12 months.
Showing 23401–23420 of 29,298 recalls
Recalled Item: 1/8 in. Double Trocar with Wound Drain Curved Trocar with Recalled by...
The Issue: Stryker Instruments is voluntarily recalling the CBCII Wound Drains and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 3/16 in. Double Trocar with Wound Drain Curved Trocar with Recalled by...
The Issue: Stryker Instruments is voluntarily recalling the CBCII Wound Drains and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 1/4 in. Double Trocar with Wound Drain Curved Trocar with Recalled by...
The Issue: Stryker Instruments is voluntarily recalling the CBCII Wound Drains and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Diamedix Is-CMV IgG Test Kit Recalled by Diamedix Corporation Due to Product...
The Issue: Product contained an incorrect substrate.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CSA Medical truFreeze Console- Cryosurgical Unit Cryogenic Surgical Device...
The Issue: TruFreeze Console caused a higher rate of liquid nitrogen (cryogen) to be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Universal Charger Product Usage: The Stryker Universal Battery Charger is...
The Issue: The Stryker Universal Battery Charger is not transmitting usage data to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dual Delivery 4DD-1 of GYC-1000 Green Laser Photocoagulator system GYC4DD-1:...
The Issue: Accessories to the GYC-1000 laser were missing Laser Aperture labels.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Light Sheer Desire Diode Laser System with XC Handpiece Accessory options....
The Issue: Device software treatment preset parameters for the XC treatment handpiece...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sentec Recalled by SenTec AG Due to SenTec is voluntarily replacing V-Sign...
The Issue: SenTec is voluntarily replacing V-Sign Sensors 2 due to pre-mature...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TIGERPAW System II Recalled by Laax, Inc. Due to Increase of field reports...
The Issue: Increase of field reports involving issues with the TIGERPAW System II...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TIGERPAW System II Recalled by Laax, Inc. Due to Increase of field reports...
The Issue: Increase of field reports involving issues with the TIGERPAW System II...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Endophotocoagulation Delivery 4EP-1 of GYC-1000 Green Laser Photocoagulator...
The Issue: Accessories to the GYC-1000 laser were missing Laser Aperture labels.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Hamilton-G5 Ventilators with software versions V2.40/2.41 Catalog numbers...
The Issue: Customer reports that the ventilator display can freeze. Ventilation...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Synthes Small Battery Drive (SBD) Oscillating Saw Attachment Part Number:...
The Issue: The potential exists for the Oscillating Saw Attachment to disengage from...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Covidien Trellis 6 and Trellis 8 Peripheral Infusion Systems Recalled by...
The Issue: Medtronic is conducting a voluntary recall of all former Covidien Trellis 6...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Homocysteine test system - Homocysteine Reagent. 05385415190 Recalled by...
The Issue: Customers complained about under-recovery of non-Roche controls and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Edwards Lifesciences Fem-Flex II Femoral Arterial Cannula 8 Recalled by...
The Issue: Edwards Lifesciences is recalling Fem-Flex II Pediatric Femoral Arterial...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips DigitalDiagnost Release 4.0.3 Recalled by Philips Electronics North...
The Issue: The system is designed to emit a beep upon termination of an exposure....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: CD123 (9F5) PE Catalog number 649453 Analyte Specific Reagent Recalled by BD...
The Issue: One lot of BD CD123 PE (ASR) has been determined to contain a low amount of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ADVIA Chemistry Lipase Reagent Recalled by Siemens Healthcare Diagnostics,...
The Issue: Siemens internal investigation confirmed that current contamination...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.