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. 2,367 recalls have been distributed to Wyoming in the last 12 months.
Showing 26761–26780 of 48,219 recalls
Recalled Item: Oxytocin 20 units added to 1000 mL Lactated Ringer's Injection Recalled by...
The Issue: Subpotent Drug
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Oxytocin 30 units added to 500 mL 5% Dextrose/Lactated Ringer's Recalled by...
The Issue: Subpotent Drug
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Oxytocin 20 units added to 1000 mL Lactated Ringer's Injection Recalled by...
The Issue: Subpotent Drug
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Oxytocin 30 units added to 500 mL Lactated Ringer's USP in 500 mL bag Rx...
The Issue: Subpotent Drug
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Oxytocin 15 units added to 250 mL Lactated Ringer's Injection USP in 250 mL...
The Issue: Subpotent Drug
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Oxytocin 40 units added to 1000 mL Lactated Ringer's USP in 1000 mL bag Rx...
The Issue: Subpotent Drug
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Sterile Water for Injection Recalled by Pfizer Inc. Due to Non-Sterility:...
The Issue: Non-Sterility: cracked or chipped glass at the neck of Sterile Water for...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Baxter Amia Automated Peritoneal Dialysis Set with Cassette Recalled by...
The Issue: The firm received increased customer complaints for Missing Red Line,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Electric Wheelchair bases: a) C300 b) C350 c) C400 d) C500 Recalled by...
The Issue: There is a potential failure of the top plate assembly, which is the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Electric Wheelchairs: a) C300 CORPUS II b) C350 CORPUS II Recalled by...
The Issue: There is a potential failure of the top plate assembly, which is the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: The ELAN 4 Air System is intended for high speed cutting Recalled by...
The Issue: The ELAN 4 Air System was released to the market place prior to an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Elekta ERGO++ Product Usage: ERGO is often used for stereotactic treatments....
The Issue: Incorrect DICOM mapping of the exported collimator or couch angles from...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AERO IOL Injection System containing 10 Z28 Cartridges per box Recalled by...
The Issue: The recommended storage temperature on the label is incorrect.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mobile Mini C-arm system Part # 1000-0001. Intended to provide Recalled by...
The Issue: OrthoScan Inc. discovered during investigation of a non-standard work flow a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mobile Mini C-arm system Part # 1000-0005. Intended to provide Recalled by...
The Issue: OrthoScan Inc. discovered during investigation of a non-standard work flow a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mobile Mini C-arm system Part # 1000-0004-FD. Intended to provide Recalled...
The Issue: OrthoScan Inc. discovered during investigation of a non-standard work flow a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 1113 Gravity Tube Set Pk/24 -SH Product Usage: The FMS Recalled by DePuy...
The Issue: Leakage of FMS gravity tub sets (281113) at the bulb and tube connection
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Mobile Mini C-arm system Part # 1000-0004. Intended to provide Recalled by...
The Issue: OrthoScan Inc. discovered during investigation of a non-standard work flow a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Syngo.via systems with SW VB20A Recalled by Siemens Medical Solutions USA,...
The Issue: A software update was released on August 22, 2017. Performing this software...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Orange Flavor Immune Support Dietary Supplement Effervescent Tablets 10...
The Issue: The label does not list "Sodium" in the ingredient statement.
Recommended Action: Do not consume. Return to store for a refund or discard.