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Pfm Medical Inc

Complete recall history across all FDA and CPSC categories — 9 total recalls

Pfm Medical 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 (9)

FDA medical device enforcement actions by Pfm Medical Inc

Date Product Reason Class
Oct 20, 2014 ASEPT 2000 ml Drainage Bag, Ref No. 622280 Product Usage: The ASEPT Drain... PFM Medical is recalling catheters and other medical devices because they may... Class II
Oct 20, 2014 ASEPT 600 ml Drainage Kit, Ref No. 622287, M7052 Product Usage: The ASEPT ... PFM Medical is recalling catheters and other medical devices because they may... Class II
Oct 20, 2014 Rapid Centesis Catheter, 5 Fr x 7 cm Catheter, Ref No. M7513 Product Usage... PFM Medical is recalling catheters and other medical devices because they may... Class II
Oct 20, 2014 Thoracentesis & Paracentesis Procedure Tray, Ref No. M7553, 850004 Product... PFM Medical is recalling catheters and other medical devices because they may... Class II
Oct 20, 2014 Veta Peritoneal Catheter Kit, Curled, Ref No. M7225 Product Usage: Veta P... PFM Medical is recalling catheters and other medical devices because they may... Class II
Oct 20, 2014 Micro Introducer Kit, 5F Micro Introducer Kit, Ref No. M4005 Product Usage... PFM Medical is recalling catheters and other medical devices because they may... Class II
Oct 20, 2014 ASEPT Peritoneal Drainage System, Ref No. P09080002 Product Usage: The pf... PFM Medical is recalling catheters and other medical devices because they may... Class II
Oct 20, 2014 6F x 60 cm Dual Lumen CT PICC, Ref No. PFM2CT6D Product Usage:The PFM CT P... PFM Medical is recalling catheters and other medical devices because they may... Class II
Oct 20, 2014 ASEPT Pleural Drainage System, Pleural Drainage Catheter Kit, Ref No. P090800... PFM Medical is recalling catheters and other medical devices because they may... 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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