Product Recalls in Montana
Product recalls affecting Montana — including food, drugs, consumer products, medical devices, and vehicles distributed to Montana. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,359 recalls have been distributed to Montana in the last 12 months.
Showing 30161–30180 of 48,326 recalls
Recalled Item: Elcam Minimal Residual Volume Luer-activated Swabable-stockcock (MRVLS) 4w...
The Issue: The stopcock was found to have punctures.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PGCL [poly (glycolide-co-caprolactone)] Absorbable Suture Recalled by CP...
The Issue: The tensile strength minimum as directed by USP <881> was not met over the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Smith & Nephew Dyonics Saw Blade Recalled by Smith & Nephew, Inc. Due to The...
The Issue: The single use devices are provided sterile and do not have an expiration...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Smith & Nephew Dyonics Saw Blade Recalled by Smith & Nephew, Inc. Due to The...
The Issue: The single use devices are provided sterile and do not have an expiration...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Smith & Nephew Dyonics Saw Blade Recalled by Smith & Nephew, Inc. Due to The...
The Issue: The single use devices are provided sterile and do not have an expiration...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Smith & Nephew Dyonics Saw Blade Recalled by Smith & Nephew, Inc. Due to The...
The Issue: The single use devices are provided sterile and do not have an expiration...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Smith & Nephew Dyonics Saw Blade Recalled by Smith & Nephew, Inc. Due to The...
The Issue: The single use devices are provided sterile and do not have an expiration...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Smith & Nephew Dyonics Saw Blade Recalled by Smith & Nephew, Inc. Due to The...
The Issue: The single use devices are provided sterile and do not have an expiration...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Final Fit Software Version 1.11 and 1.12 Recalled by Nidek Inc Due to During...
The Issue: During treatment planning, the procedure was programmed with an unintended...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Micropuncture Check-Flo Performer Introducer Set Recalled by Cook Inc. Due...
The Issue: Devices using a specific hemostatic valve design, to as a blue valve or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TriForce Peripheral Crossing Set Recalled by Cook Inc. Due to Devices using...
The Issue: Devices using a specific hemostatic valve design, to as a blue valve or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Check-Flo Hemostasis Assembly Recalled by Cook Inc. Due to Devices using a...
The Issue: Devices using a specific hemostatic valve design, to as a blue valve or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Check-Flo Performer Introducer Recalled by Cook Inc. Due to Devices using a...
The Issue: Devices using a specific hemostatic valve design, to as a blue valve or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Check-Flo Performer Introducer Set Recalled by Cook Inc. Due to Devices...
The Issue: Devices using a specific hemostatic valve design, to as a blue valve or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Check-Flo Introducer Hausdorf-Lock Atrial Recalled by Cook Inc. Due to...
The Issue: Devices using a specific hemostatic valve design, to as a blue valve or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Flexor Radial Access Set Recalled by Cook Inc. Due to Devices using a...
The Issue: Devices using a specific hemostatic valve design, to as a blue valve or...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SHBG IMMULITE 2000/IMMULITE 2000 XPi For the in vitro diagnostic Recalled by...
The Issue: Certain lots of Sex Hormone Binding Globulin (SHBG) do not meet the thirty...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 882480: BrightView designed for single or dual detector nuclear imaging...
The Issue: Four issues: 1. Motion controller problem stops scan and no data image...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 882482: BrightView XCT 882454 BrightView X upgrade to XCT Recalled by...
The Issue: Four issues: 1. Motion controller problem stops scan and no data image...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 882478: BrightView X designed for single or dual detector nuclear Recalled...
The Issue: Four issues: 1. Motion controller problem stops scan and no data image...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.