Berchtold Corp.
Complete recall history across all FDA and CPSC categories — 5 total recalls
Berchtold 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 (5)
FDA medical device enforcement actions by Berchtold Corp.
| Date | Product | Reason | Class |
|---|---|---|---|
| Apr 19, 2016 | Surgical Table Cushion (HybriGel Pads) HybrGel Pads are an optional accessor... | The Surgical Table Cushion (HybriGel Pads) could potentially contain staples ... | Class II |
| Sep 23, 2015 | TELETOM EQUIPMENT MANAGEMENT SYSTEM 4 and 6 series TELETOM is designed for u... | During the use of the TELETOM Series 4 & 6 there is potential for the control... | Class II |
| Mar 12, 2013 | Hand Controls for Operon D750, D752, D760, D820 and D850 The hand controls... | The firm received complaints for unintended movements. | Class II |
| Jul 10, 2012 | Chromovision High Definition (HD) Wireless Camera, Pt # CC-9715900. Visual... | Defective camera: There is a possibility that the connection of the wires to ... | Class III |
| Apr 16, 2012 | OPERON D850 Surgical Table Product Usage: Surgical Table | Table was not lowering. | 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.
Yes. You can search for any company using the firm/manufacturer pages for each category: Food Firms, Drug Firms, Device Firms, or Product Manufacturers. You can also use the search functionality on any browse page to find recalls by company name.
Explore More Recalls
Search recalls by category, state, reason, or firm across all our databases.