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PSC Industries Inc

Complete recall history across all FDA and CPSC categories — 8 total recalls

PSC Industries 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 (8)

FDA medical device enforcement actions by PSC Industries Inc

Date Product Reason Class
Jun 5, 2012 Button Switchpens, w/Extendable Needle Electrode 10 mm Exposure, Single Use ... The Tyvek pouch label for this device states: 'with holster'; however, this ... Class II
Jun 5, 2012 Button Switchpens, w/Extendable Needle Electrode 2 mm Exposure Single Use Ele... The carton label for this device has the manufacturer symbol where the expira... Class II
Jun 1, 2012 Bayonet Forceps 8.25 (209.6 mm) 0.5mm Tips, Sterile Single Use Surgical/Bipol... Firm officials reported to CIN-DO that for this device, in the labeling on t... Class II
Jun 1, 2012 Bayonet Forceps 7.-1/8 (181.0mm) 0.75mm Insulated Tips, Sterile Single Use S... Firm officials reported to CIN-DO that the outer carton label of this sterile... Class II
Jun 1, 2012 Bayonet Forceps 8.5" (215.9mm) Serrated 1.0 mm Tips Electrosurgical/Monopolar... Firm officials reported to CIN-DO that their Electrosurgical Monopolar Reusab... Class II
Jun 1, 2012 Irrigating Bayonet Forceps 8.25" (209.6 mm) 1.5 mm Tips, Electrosurgical Irri... Firm officials reported to CIN-DO that for this device, in the labeling on t... Class II
Jun 1, 2012 Bayonet Forceps 7.75" (196.9 mm) 0.5 mm Tips Non-Stick Electrosurgical/Bipo... Firm officials reported to CIN-DO that their Bipolar Bayonet Forceps 7.75" a... Class II
Jun 1, 2012 Bayonet Forceps 7.-1/8 (181.0mm) 0.75mm Non-Insulated Tips, Sterile Single Us... Firm officials reported to CIN-DO that for this device, in the labeling on t... 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.

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