Loading...
Loading...
All product recalls associated with Apace KY LLC.
Total Recalls
59
Past Year
3
Class I (Serious)
0
Most Recent
Sep 2025
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.
Labeling; Label Mix up; cartons labeled as Amantadine HCl 100 mg Capsules contain unit dose blister cards of Cyclobenzaprine HCl Tablet, USP 5 mg
Labeling; Label Mix up; cartons labeled as Amantadine HCl 100 mg Capsules contain unit dose blister cards of Cyclobenzaprine HCl Tablet, USP 5 mg
LGS Industries Inc (LGS) is recalling certain model year 2017 Look, Pace, and Cargo Express cargo trailers manufactured October 24, 2016, to November 8, 2016. Due to insufficient welds, the bracket that attaches the torsion spring cable to the ramp door could detach from the ramp door.
Labeling: Incorrect or Missing Lot and/or Exp Date: the individual blisters are mislabeled with an incorrect lot number of 13560 rather than the correct lot number of 13650.
The clinician did not realize the monitor was in END CASE mode and was expecting audible alarms. Visual alarms continue to work normally. The firm performed a retrospective analysis of all recalls since 2011 and discovered 222 additional serial numbers were missed and were not included in the previous recall under RES 59456 (recall number Z-3032-2011).
Space Craft Mfg., Inc. (Space Craft) is recalling certain model year 2006-2013 fifth wheel and travel trailers manufactured January 1, 2006, through April 25, 2013 and equipped with Fastec-brand door locks. It may be possible to remove the key from the lock in a way that potentially jams the deadbolt.
Labeling Illegible: Some bottles labels have incomplete NDC numbers and missing strength.
This recall involves previously recalled "Innovations" and "At Home with Meijer" Roman shades and roll-up blinds that were redistributed to stores and sold to consumers after March 2010 without a repair kit. The Roman shades are made with fabric or bamboo and the roll-up blinds with bamboo. A label reading "Innovation" or "At Home with Meijer" can be found under the headrail.
SPACE CRAFT IS RECALLING CERTAIN MODEL YEAR 2006 530 AND V420 SPACE CRAFT RECREATIONAL VEHICLES EQUIPPED WITH 1200-SERIES NORCOLD REFRIGERATORS. THE POPULATION OF REFRIGERATORS BEING ADDRESSED CONTAINS EITHER A SENSING ALGORITHM OR THERMAL SWITCH TO SHUT OFF POWER TO THE REFRIGERATOR WHEN HIGH TEMPERATURES ARE DETECTED IN ORDER TO PREVENT A POTENTIAL FIRE. THE RESPONSE TIMES OF THE SENSOR ALGORITHM AND THERMAL SWITCH DEVICES TO STOP POWER ARE NOT SUFFICIENT.
This recall involves all Innovations and "At Home with Meijer" Roman shades and roll-up blinds. The Roman shades are made with fabric or bamboo and the Roll-up blinds with bamboo. A label reading "Innovation" or "At Home with Meijer" can be found under the headrail.
Potential for monitor to shut down and not being able to power on again.
Potential for monitor to shut down and not being able to power on again.
Potential for monitor to shut down and not being able to power on again.
This recall involves all Faux Suede room darkening Roman shades with style number 12810A. The shades were sold in Ivory, Taupe, Gold, Plum, Wine Red, Midnight Blue, Moss Green and Dark Brown and have a head rail that measures 23, 27, 31, 35, 39 43 or 48 inches. The shades have a sticker on the head rail with the letters "WS" and "style 12810A" is printed on the packaging box.
The Spacelabs Medical Flat Panel Display, Model 94260-19 may fail prematurely and causing the screen to go blank. This inability to view data may result in delayed patient treatment.
The Spacelabs Medical Integrated ECG Cables, PN: 700-0008-22, 700-0008-23, 700-0008-24, and 700-0008-25 will not withstand the high voltage of a defibrillation shock.
Users may experience difficulty turning the control knob to an active vapour delivery setting, or may not be able to turn on the Left Hand mounted vapouriser on the Blease Sirius Anaesthesia Systems.
The power supply of the Spacelabs Medical Flat Panel Display may fail, causing the display to go blank.
Potential for device to print out the wrong waveform data for the time indicated in the printout or display.
Potential for module to fail to obtain a NIBP reading on hypertension patients.