Product Recalls in Wyoming
Product recalls affecting Wyoming — including food, drugs, consumer products, medical devices, and vehicles distributed to Wyoming. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,448 recalls have been distributed to Wyoming in the last 12 months.
Showing 18381–18400 of 48,219 recalls
Recalled Item: Butterfly iQ Ultrasound System containing the Auto EF(Ejection Fraction)...
The Issue: Distributed without an approved 510(k)
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LivaNova Heater-Cooler System 3T - Product Usage: The Heater-Cooler 3T...
The Issue: The firm is providing validated cleaning and disinfection instructions in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Well at Walgreens Sodium Chloride Ophthalmic Ointment USP Recalled by Akorn,...
The Issue: Presence of Particulate Matter: Brown spots observed on the inside of the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: CVS Health Sodium Chloride Ophthalmic Ointment USP Recalled by Akorn, Inc....
The Issue: Presence of Particulate Matter: Brown spots observed on the inside of the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Sodium Chloride Ophthalmic Ointment USP Recalled by Akorn, Inc. Due to...
The Issue: Presence of Particulate Matter: Brown spots observed on the inside of the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Moonstruck Praline Pecan & Ginger Element Bar in Dark Chocolate Recalled by...
The Issue: Undeclared milk.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: R-F Injector Cannula. 18gx10cm-STERILE. REF/UDI: 257-1810/(01)00828788021496...
The Issue: Incorrect expiration date on introduction cannula packaging.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: R-F Injector Cannula. 20gx10cm-STERILE. REF/UDI: 257-2010/(01)10818788022124...
The Issue: Incorrect expiration date on introduction cannula packaging.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AmniSure ROM Test Recalled by Qiagen Sciences LLC Due to An image on the...
The Issue: An image on the associated polybag contains an incorrect rinse time of 30...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mesalamine Delayed-Release Tablets Recalled by Teva Pharmaceuticals USA Due...
The Issue: Failed Dissolution Specifications: Low out of specification dissolution...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: TCM4 Base unit Recalled by Radiometer Medical ApS Due to Reports have been...
The Issue: Reports have been received about the transcutaneous monitoring system...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Expression MR400 MRI Patient Monitoring System Model Number: 866185 Software...
The Issue: Menu selections for users to access the oxygen (O2) sensor calibration were...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: NATURAL GROCERS ALMOND CLUSTERS DK CHOCOLATE NON-GMO Recalled by Vitamin...
The Issue: Undeclared peanut and milk allergens
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: NATURAL GROCERS PEANUT CLUSTERS DK CHOCOLATE NON-GMO Recalled by Vitamin...
The Issue: Undeclared almond and milk allergens
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: TEG Manager software versions used in conjunction with TEG 5000 are 1.1.0...
The Issue: Software defect in TEG Manager impacts the displayed alert for out of range...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: QC Sets and Panels Recalled by Microbiologics Inc Due to Tests returning...
The Issue: Tests returning incorrect susceptible results. High Level Gentamicin Synergy...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: QC Sets and Panels Recalled by Microbiologics Inc Due to Tests returning...
The Issue: Tests returning incorrect susceptible results. High Level Gentamicin Synergy...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LYFO-DISK Enterococcus faecalis derived from ATCC 51299 In Vitro Diagnostic...
The Issue: Tests returning incorrect susceptible results. High Level Gentamicin Synergy...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: QC Sets and Panels Recalled by Microbiologics Inc Due to Tests returning...
The Issue: Tests returning incorrect susceptible results. High Level Gentamicin Synergy...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: KWIK-STIK Recalled by Microbiologics Inc Due to Tests returning incorrect...
The Issue: Tests returning incorrect susceptible results. High Level Gentamicin Synergy...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.