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Panoramic Rental Corp.

Complete recall history across all FDA and CPSC categories — 3 total recalls

Panoramic Rental Corp. appears in recall records across 1 category. This page consolidates all FDA food, drug, and medical device enforcement actions, plus CPSC consumer product recalls associated with this company. Recall data is sourced from openFDA and CPSC public databases.

Device Recalls (3)

FDA medical device enforcement actions by Panoramic Rental Corp.

Date Product Reason Class
Jul 14, 2017 PC-1000, PC-1000/Laser1000, Model Numbers 800724-2 & 800724-3 The lift motor used to raise and lower the overhead chassis will wear if not ... Class II
Aug 19, 2016 Panoramic X-ray Model PC-1000, Laser-1000 packed in a crate Product Usage:... Panoramic Corporation is performing a voluntary Medical Device Correction on ... Class II
Jun 4, 2015 Panoramic X-ray Model PC-1000 The PC-1000 will enable the user to take pan... Jackscrew nut part failure potentially leading to device malfunction and pati... Class II

Frequently Asked Questions

A high number of recalls does not necessarily indicate that a company is unsafe. Large manufacturers that produce thousands of products across multiple categories will statistically appear in recall databases more frequently. What matters more is the severity of each recall (Class I being the most serious), the speed of response, and whether the company proactively identified and addressed the issue. Companies with robust safety programs often catch problems earlier.

Food, drug, and medical device recall data comes from the FDA's openFDA enforcement database, which contains all FDA enforcement reports. Consumer product recall data comes from the U.S. Consumer Product Safety Commission (CPSC). Both sources are public government databases that are updated regularly. RecallCheck aggregates these sources to provide a unified view of a company's recall history.

The FDA classifies recalls into three categories. Class I is the most serious — there is a reasonable probability that use of or exposure to the product will cause serious adverse health consequences or death. Class II means the product may cause temporary or medically reversible health problems, or the probability of serious consequences is remote. Class III is the least serious — the product is unlikely to cause adverse health consequences. CPSC product recalls do not use this classification system.

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