Welch Allyn Inc
Complete recall history across all FDA and CPSC categories — 5 total recalls
Welch Allyn Inc 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 Welch Allyn Inc
| Date | Product | Reason | Class |
|---|---|---|---|
| Jul 20, 2021 | Braun ThermoScan PRO 6000 Ear Thermometer-indicated for the intermittent meas... | If the device is exposed to fluid ingress and is used before the cleaning flu... | Class II |
| Apr 22, 2021 | ProBP 3400 Digital Blood Pressure Device ((handheld, desk mount, wall mount m... | Potential Risk of fluid ingress to the power supplies, resulting in risk of ... | Class II |
| Apr 22, 2021 | GS777 Wall Transformer Model: 77710 Intended Use: The GS777 Wall ... | Potential Risk of fluid ingress to the power supplies, resulting in risk of ... | Class II |
| Feb 27, 2017 | Welch Allyn ProBP 2400 Digital Blood Pressure Device #2400, REF 901096, Rx ON... | A defective electrical component in the battery charging circuit in two lots ... | Class II |
| Oct 2, 2015 | Welch Allyn KleenSpec Corded Illumination System, Vaginal Speculum Lighting S... | The firm became aware that the KleenSpec¿ 788 Corded Illuminator has the pote... | 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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