B. Braun recalls 23,688 bags of Lactated Ringer's Injection over particulate matter
FDA classifies the nationwide recall as Class I, its most serious category.
Recalls & Safety Alerts in Pennsylvania
Every recalls & safety alerts report published for Pennsylvania, newest first.
Olympus Recalls PowerSeal 5 mm Sealer Over Labeling Error
FDA classifies recall of 335 units as Class II due to incorrect labeling on outer shelf boxes.
FDA Class II Recall Issued for Tobii Dynavox Speech Generating Device
The FDA has classified a recall of the TD Navio Midi speech generating device as Class II due to potential battery damage that could cause internal short circuit.
Bazzini LLC Recalls Dark Chocolate Coconut Almond Bites Over Undeclared Peanuts
The FDA has classified the recall as Class I, indicating a reasonable probability of serious harm or death.
FDA Terminates Recall of Galliker Dairy Ice Cream Mix
The Food and Drug Administration has closed its recall of DQ Chocolate Reduced Fat Ice Cream Mix previously recalled for metal shavings.
FDA Reports Ongoing Recall of Quantum Rehab Powered Wheelchairs Over Software Issue
An ongoing recall covers 1,102 Quantum Outback powered wheelchairs whose controller software may cause unexpected braking or system crashes.
FDA Enforcement Report Details Ongoing Recall of Quantum Rehab Powered Wheelchairs
An ongoing Class II recall covers 1102 Quantum Rehab powered wheelchairs due to a controller software issue that can trigger unexpected braking or system crashes.
Olympus Recalls 3,241 Ellik Evacuator Units Over Sterilization Instructions
An FDA enforcement report says some sterilization parameters in the instructions for use may not consistently render the urological devices adequately sterile.