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. 2,277 recalls have been distributed to Montana in the last 12 months.
Showing 45661–45680 of 48,326 recalls
Recalled Item: Philips HeartStart XL+ Defibrillator/Monitor Model number: 861290 The...
The Issue: Philips HeartStart XL+ Defibrillator/Monitor may become locked out of...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ELECTROLASE(R) HYFRECATOR(R) ELECTRODES - BLUNT Recalled by ConMed...
The Issue: Some devices had broken through the seal of the sterile pouch. ConMed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ELECTROLASE HYFRECATOR(R) ELECTRODES - SHARP Recalled by ConMed Corporation...
The Issue: Some devices had broken through the seal of the sterile pouch. ConMed...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Varian Eclipse Treatment Planning System for Radiotherapy Recalled by Varian...
The Issue: The calculation of dose dynamic plans containing different energy fields is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Prism Medical C-Series Carry Bar Recalled by Prism Medical Services USA Due...
The Issue: The firm replaced the recalled carry bar with a plastic insert with a carry...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lactated Ringer's and 5% Dextrose Injection Recalled by Hospira Inc. Due to...
The Issue: Non-Sterility: Confirmed customer complaint of product contaminated with mold.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: KY SENSITIVE TM JELLY Personal Lubricant. The product is packaged Recalled...
The Issue: This product is not cleared for marketing in the US.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Puritan Bennett 700 Series Ventilators (PB740 and PB760) PB700 Series...
The Issue: Covidien is correcting labeling to clarify the operational life of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Puritan Bennett 840 Series Ventilator PB840 Operators Manual Addendum PN...
The Issue: Covidien is correcting labeling to clarify the operational life of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Proplege Coronary Sinus Catheter model PR9 Recalled by Edwards Lifesciences,...
The Issue: Edwards Lifesciences is recalling certain Proplege Coronary Sinus Catheter,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KY SilkE Vaginal Moisturizer and Personal Lubricant. The product is Recalled...
The Issue: This product is not cleared for marketing in the US.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KY TINGLING JELLY Personal Lubricant. The product is packaged into Recalled...
The Issue: This product is not cleared for marketing in the US.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: HLD System Recalled by Cenorin, LLC Due to The temperature sensor/control...
The Issue: The temperature sensor/control system in the HLD Systems Model 610 may...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Stelkast Cross-over Acetabular Shell and Liner Hip System Recalled by...
The Issue: Firm was made aware of incidents relating to the difficulty of properly...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: D3000I Advantage Drive System Recalled by Linvatec Corp. dba ConMed Linvatec...
The Issue: The Membrane Switch Panel ( to as "front panel" of the component part number...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: D3000 Advantage Drive System Recalled by Linvatec Corp. dba ConMed Linvatec...
The Issue: The Membrane Switch Panel ( to as "front panel" of the component part number...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sodium Sulfacetamide 10% and Sulfur 5% Lotion Recalled by Mission Pharmacal...
The Issue: Superpotent: Drug product active ingredients were formulated incorrectly...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Terazosin Hydrochloride Capsules Recalled by Teva Pharmaceuticals USA, Inc....
The Issue: Presence of Foreign Tablets/Capsules: Recall is being conducted due to a...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Crest PRO-HEALTH CPC Antigingivitis/Antiplaque Oral Rinse Recalled by...
The Issue: Cross Contamination with Other Products: Product was mixed with another type...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Plastic bottle containing 3.5 mL of IgG FITC Conjugate Product Recalled by...
The Issue: Affected products have a labeled expiration date of one year too long.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.