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All product recalls associated with COACHMEN.
Total Recalls
1000
Past Year
896
Class I (Serious)
125
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.
Forest River, Inc. (Forest River) is recalling certain 2023-2024 Coachmen Concord motorhomes. The lower control arm bracket may fail and cause the axle to rotate or detach, resulting in a loss of vehicle control.
Failed Stability Specifications: Out of specification for blend uniformity.
an out of specification result obtained during routine stability testing for Impurities. There is a remote possibility that use of this product could cause a medically reversible or transient adverse health consequences.
Listeria monocytogenes. The recalled Cotija cheese was repackaged into finished RTE Sprig and Sprout Ham and Cotija Torta Sandwich on Telera Roll.
This recall involves CableMod's 12VHPWR Angled Adapters, models V1.0 and V1.1, that plug into a graphics processing unit's power port at either a 90-degree or a 180-degree angle. Model V1.1 has a stabilizing pin on the side of the male connector. The adapters were sold in black, blue, gold, green, orange, pink, purple, red, silver, and white, and "CableMod" appears on the side of the adapter. The adapters came in two variations to accommodate power port orientation: Variation A and Variation B. The 90-degree angle adapter is "L" shaped: The V1.0 model measures about 36 mm long, 21mm wide and 21 mm deep; and the V1.1 model measures about 36 mm long, 21 mm wide and 22 mm deep. The 180-degree angle adapter is "U" shaped: The V1.0 model measures 41.5 mm long, 21 mm wide and 17.5 mm deep; and the V1.1 measures about 41 mm long, 21 mm wide and 20 mm deep.
Software: If the user excludes voxels from the Gamma calculation that are below a dose threshold (Suppress gamma calculation), the Gamma Passing Rate (GPR) calculated for individual ROIs is not correct. The GPR calculated by VERIQA overestimates the correct GPR. The evaluation can therefore show false positive results.
Due to insufficient mounting force the stability of surgical light system cannot be guaranteed.
This recall involves two styles of 100% polyester hooded children's bathrobes; the dinosaur style in green, rose red and orange, and the shark style in blue, pink, yellow and gray. The bathrobes have attached belts and patch pockets. The size, manufacturer information and care instructions are printed on sewn-in labels inside the left inseam of the robes. They were sold in sizes 2-3 years, 3-5 years, and 6-8 years.
Four lots of Access Total T4 reagent lots demonstrated imprecision outside of the 10% specification which may result in erroneous or delayed results.
Due to a change in the safety clips for the heated eye masks, the wires to the safety clips may detach as a result of tugging and pulling and may cause a short in the heating element of the mask and could potentially cause burn injuries.
On 07 February 2024 Beckman Coulter made the decision to conduct a field action on Access Substrate (81906) lots: 234600, 337984, 338040, 338214, 338229, 338289, 338322, 338333, 338451, 338587, and 338538. Beckman Coulter has identified that Access Substrate bottles in the identified lots were released from manufacturing without labels. Missing label may cause some patient results reporting delay but will not cause any errorreous results. However, because labs are required to have redundancy such that delay would not significantly impact clinical management and because the defect is easily recognized by the user, the probability of harm is remote.
Medtronic is writing to inform you of incorrect labeling for three manufactured lots of the DLP Vessel Cannulae for the model and lot numbers listed above.
L. mono contamination
cGMP Deviations: Products were stored outside the drug label specifications.
cGMP Deviations: Products were stored outside the drug label specifications.
cGMP Deviations: Products were stored outside the drug label specifications.
L. mono contamination
L. mono contamination
Generator may fail due to a potential short circuit in the Printed Circuit Board Assembly (PCBA) in PoInt EVR (Power Invertor). If a short circuit occurs, it will cause the fuses to trip and the system will become non-functional due to power loss, resulting in a potential delay of procedure or termination of procedure.
Generator may fail due to a potential short circuit in the Printed Circuit Board Assembly (PCBA) in PoInt EVR (Power Invertor). If a short circuit occurs, it will cause the fuses to trip and the system will become non-functional due to power loss, resulting in a potential delay of procedure or termination of procedure.