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All product recalls associated with Lacrimedics Inc.
Total Recalls
1000
Past Year
1000
Class I (Serious)
127
Most Recent
Jan 2026
Data from FDA, USDA, CPSC, and NHTSA public records. Recall counts vary by company size, industry, and reporting practices. Always check official sources for current information.
The sterile pouch seal may contain channels that could affect the seal integrity and potentially compromise sterility.
The sterile pouch seal may contain channels that could affect the seal integrity and potentially compromise sterility.
Optic nerve head angiography scan to be turned off due to its distribution without pre-market clearance.
Product lacks premarket clearance.
CGMP Deviation: Difficulty dispensing/does not dispense or dispensing liquid instead of foam.
Failed Impurities/Degradation Specifications
Volta Power Systems LLC (Volta) is recalling certain adaptor harnesses, part number 100001146. The wire harness may have been built incorrectly, resulting in the loss of over-current protection.
Undeclared wheat allergen.
The recall involves EGL and ACE branded Youth ATVs, models MADIX 125 and D110. The name of the vehicle is printed on a label located on both sides of the vehicle. The model number is stamped into the metal plate located on the left side, under the rear body. The ATVs were sold as either Age 12+ or Age 16+. The ATVs have a label under the model number, stating: "This ATV is subject to EGL MOTOR INC's action plan approved by U.S. Consumer Product Safety Commission."
This recall involves Bella residential elevators manufactured from 2009 to 2021. Models include Symmetry IGD, Hydraulic, and Winding Drum Elevators. The Symmetry brand name is located on the elevators' controllers. The elevators are used in consumers' homes.
This recall involves Inclinator residential elevators manufactured from 1979 through 2021. Models include: Winding Drum (450 - 1,000 lb.), Hydraulic Drive, Chain Drive, Traction Drive and Overhead Cable Drum. Serial numbers are located on the elevator controllers, stamped on the rails, or on the outside of the drum for Winding Drum units. The elevators are used in consumers' homes.
Play-Mor Trailers, Inc. (Play-Mor) is recalling certain 2017-2020 3 Room Actor, 2 Room Actor, 2 Room Office, Hair and Makeup, Restroom, 2020 Single Actor, 2019-2020 Motorsport SUV, and 2017 199 Camping Trailer, and Custom BBQ trailers equipped with Winntec model 6020 two-stage propane regulators. The regulator may fail, causing an increase in propane pressure.
Lack of Assurance of Sterility
cGMP deviations
It was found that the irradiated x-ray may exceed the xray radiation dose rate specified in CFR 1020.32 in some specific case of fluoroscopic mode due to inadequate adjusting criteria in installation.
It was found that the irradiated x-ray may exceed the xray radiation dose rate specified in CFR 1020.32 in some specific case of fluoroscopic mode due to inadequate adjusting criteria in installation.
It was found that the irradiated x-ray may exceed the xray radiation dose rate specified in CFR 1020.32 in some specific case of fluoroscopic mode due to inadequate adjusting criteria in installation.
CGMP Deviations
Failed Dissolution Specifications; Low Out of specification (OOS) results for dissolution.
The product was released for distribution without passing sterilization results, which could potentially lead to insufficient sterility of the product. The highest severity risk is infection leading to surgical intervention.