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All product recalls associated with Cell Distributors.
Total Recalls
1000
Past Year
99
Class I (Serious)
84
Most Recent
Dec 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: Not elsewhere classified; product labeling lacks a NDC number, net weight information and does not contain the Drug Facts Panel.
This recall involves Amphenol UTX PV model connectors sold with solar panels. The electrical connectors are used to connect various types of photovoltaic solar panels to the electrical connection system. The connectors have a black plastic exterior with "Amphenol" and "UTX PV" stamped on the end. They consist of a male pin on one end and a female socket on the other end.
Microbial Contamination of Non-Sterile Products: potential of an elevated bioburden with identification of objectionable organisms.
Labeling: Incorrect or Missing Package Insert: product lots packaged with an out-of-date insert.
Thor Motor Coach (TMC) is recalling certain 2017 Chateau, Freedom Elite, and Four Winds Motorhomes. The sofa may not have a seat belt for the middle seating position.
Thor Motor Coach (TMC) is recalling certain 2014-2015 ACE, Hurricane, Challenger, Daybreak, Miramar, Outlaw, and Windsport motorhomes. These vehicles have windshield wiper systems that may have been improperly installed and secured, possibly causing the wipers to fail during use.
H&H Sports Protection (H&H) is recalling certain TORC T-55 V2 low profile half helmets, sizes XS, S, M, L, XL, XXL. These helmets may not adequately protect the wearer in the event of a head impact during a motorcycle crash. Additionally, the helmets may not stay secured to head during a motorcycle crash. As such, these helmets fail to comply with the requirements of Federal Motor Vehicle Safety Standard (FMVSS) number 218, "Motorcycle Helmets."
Cross-contamination with other products -Related Substances test for Rivastigmine Tartrate Capsules USP, 1.5 mg showed a peak for Ranitidine.
CGMP Deviations: an expired active ingredient was used in the manufacture of these recalled lots.
Chemical Contamination
The firm was notified by their supplier that various cheese products they received were contaminated by Listeria monocytogenes.
The firm was notified by their supplier that various cheese products they received were contaminated by Listeria monocytogenes.
The firm was notified by their supplier that various cheese products they received were contaminated by Listeria monocytogenes.
The firm was notified by their supplier that various cheese products they received were contaminated by Listeria monocytogenes.
The firm was notified by their supplier that various cheese products they received were contaminated by Listeria monocytogenes.
The firm was notified by their supplier that various cheese products they received were contaminated by Listeria monocytogenes.
The firm was notified by their supplier that various cheese products they received were contaminated by Listeria monocytogenes.
The firm was notified by their supplier that various cheese products they received were contaminated by Listeria monocytogenes.
The firm was notified by their supplier that various cheese products they received were contaminated by Listeria monocytogenes.
The firm was notified by their supplier that various cheese products they received were contaminated by Listeria monocytogenes.