Customed, Inc
Complete recall history across all FDA and CPSC categories — 682 total recalls
Customed, 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 (682)
FDA medical device enforcement actions by Customed, Inc. Showing most recent 50.
| Date | Product | Reason | Class |
|---|---|---|---|
| Jan 7, 2016 | Catalog Number: 900277 SUCTION CATHETER TRAY 14FR WITH SODIUM CHLORIDE 0.9%... | Recall initiated due to inadequate validation/qualification of sterilization ... | Class II |
| Jan 7, 2016 | Catalog Number: 9002940 OBSTETRICAL SURGICAL PACK Used by medical staff to... | Recall initiated due to inadequate validation/qualification of sterilization ... | Class II |
| Jan 7, 2016 | Catalog Number: 900010 SUTURE REMOVAL KIT Used by medical staff to perform ... | Recall initiated due to inadequate validation/qualification of sterilization ... | Class II |
| Jan 7, 2016 | Catalog Number: 9001933 OPHTALMIC SURGICAL PACK Used by medical staff to ... | Recall initiated due to inadequate validation/qualification of sterilization ... | Class II |
| Jan 7, 2016 | Catalog Number: 900169 UNIVERSAL SURGICAL PACK Used by medical staff to p... | Recall initiated due to inadequate validation/qualification of sterilization ... | Class II |
| Jan 7, 2016 | Catalog Number: 9001296 PREMIUM LAPAROTOMY PACK Used by medical staff to p... | Recall initiated due to inadequate validation/qualification of sterilization ... | Class II |
| Jan 7, 2016 | Catalog Number: 9001738 UROLOGY SURGICAL PACK Used by medical staff to pe... | Recall initiated due to inadequate validation/qualification of sterilization ... | Class II |
| Jan 7, 2016 | Catalog Number: 9002193 SHOULDER ARTHROSCOPY SURGICAL PACK Used by medical... | Recall initiated due to inadequate validation/qualification of sterilization ... | Class II |
| Jan 7, 2016 | Catalog Number: 9002469 BASIC SURGICAL PACK IV Used by medical staff to p... | Recall initiated due to inadequate validation/qualification of sterilization ... | Class II |
| Jan 7, 2016 | Catalog Number: 9002510 UROLOGY SURGICAL PACK Used by medical staff to pe... | Recall initiated due to inadequate validation/qualification of sterilization ... | Class II |
| Jan 7, 2016 | Catalog Number: 900629 STERILE OR CLOTH TOWEL BLUE Used by medical staff t... | Recall initiated due to inadequate validation/qualification of sterilization ... | Class II |
| Jan 7, 2016 | Catalog Number: 900403 CESAREAN SECTION SURGICAL PACK Used by medical sta... | Recall initiated due to inadequate validation/qualification of sterilization ... | Class II |
| Jan 7, 2016 | Catalog Number: 9001198 WOUND MANAGE II Used by medical staff to perform s... | Recall initiated due to inadequate validation/qualification of sterilization ... | Class II |
| Jan 7, 2016 | Catalog Number: 900548A PERY-GYN SURGICAL PACK Used by medical staff to pe... | Recall initiated due to inadequate validation/qualification of sterilization ... | Class II |
| Jan 7, 2016 | Catalog Number: 900450 LAPAROTOMY SURGICAL PACK Used by medical staff to ... | Recall initiated due to inadequate validation/qualification of sterilization ... | Class II |
| Jan 7, 2016 | Catalog Number: 9002614 HIP AND KNEE REPLACEMENT SURGICAL PACK Used by med... | Recall initiated due to inadequate validation/qualification of sterilization ... | Class II |
| Jan 7, 2016 | Catalog Number: 9001574 LEGGINS 30X42 W/7" CUFF Used by medical staff to p... | Recall initiated due to inadequate validation/qualification of sterilization ... | Class II |
| Jan 7, 2016 | Catalog Number: 900278 URETHRAL CATHETER TRAY 14FR Used by medical staff ... | Recall initiated due to inadequate validation/qualification of sterilization ... | Class II |
| Jan 7, 2016 | Catalog Number: 900742A CARPAL TUNEL LARGE SURGICAL PACK Used by medical s... | Recall initiated due to inadequate validation/qualification of sterilization ... | Class II |
| Jan 7, 2016 | Catalog Number: 900741A ORTHO-IMPLANT SURGICAL PACK Used by medical staff ... | Recall initiated due to inadequate validation/qualification of sterilization ... | Class II |
| Jan 7, 2016 | Catalog Number: 900547 BASIC SURGICAL PACK Used by medical staff to perfo... | Recall initiated due to inadequate validation/qualification of sterilization ... | Class II |
| Jan 7, 2016 | Catalog Number: 9001154 WOUND MANAGEMENT TRAY Used by medical staff to perf... | Recall initiated due to inadequate validation/qualification of sterilization ... | Class II |
| Jan 7, 2016 | Catalog Number: 900419 LABOR & DELIVERY SURGICAL PACK Used by medical sta... | Recall initiated due to inadequate validation/qualification of sterilization ... | Class II |
| Jan 7, 2016 | Catalog Number: 900064 WOUND CLOSURE TRAY II Used by medical staff to perfo... | Recall initiated due to inadequate validation/qualification of sterilization ... | Class II |
| Jan 7, 2016 | Catalog Number: 900796 FEMORAL ANGIOGRAPHY SURGICAL PACK Used by medical ... | Recall initiated due to inadequate validation/qualification of sterilization ... | Class II |
| Jan 7, 2016 | Catalog Number: 900164 FEMORAL SURGICAL PACK Used by medical staff to pe... | Recall initiated due to inadequate validation/qualification of sterilization ... | Class II |
| Jan 7, 2016 | Catalog Number: 900168 LABOR & DELIVERY SURGICAL PACK Used by medical sta... | Recall initiated due to inadequate validation/qualification of sterilization ... | Class II |
| Jan 7, 2016 | Catalog Number: 900633 FAN FOLD SHEET 44 X 58 Used by medical staff to per... | Recall initiated due to inadequate validation/qualification of sterilization ... | Class II |
| Jan 7, 2016 | Catalog Number: 9002164 FEMORAL SURGICAL PACK Used by medical staff to per... | Recall initiated due to inadequate validation/qualification of sterilization ... | Class II |
| Jan 7, 2016 | Catalog Number: 9001402 PLASTIC SURGERY PACK Used by medical staff to perf... | Recall initiated due to inadequate validation/qualification of sterilization ... | Class II |
| Jan 7, 2016 | Catalog Number: 900618A LAPAROSCOPY-GYN SURGICAL PACK Used by medical staf... | Recall initiated due to inadequate validation/qualification of sterilization ... | Class II |
| Jan 7, 2016 | Catalog Number: 900944 CATARACT SURGICAL PACK Used by medical staff to pe... | Recall initiated due to inadequate validation/qualification of sterilization ... | Class II |
| Jan 7, 2016 | Catalog Number: 9002511 MINOR SURGICAL PACK Used by medical staff to perf... | Recall initiated due to inadequate validation/qualification of sterilization ... | Class II |
| Jan 7, 2016 | Catalog Number: 9001298 PREMIUM ARTHROSCOPY PACK Used by medical staff to ... | Recall initiated due to inadequate validation/qualification of sterilization ... | Class II |
| Jan 7, 2016 | Catalog Number: 900997 PERI-GYN SURGICAL PACK Used by medical staff to pe... | Recall initiated due to inadequate validation/qualification of sterilization ... | Class II |
| Jan 7, 2016 | Catalog Number: 9001460 REYITO PLUS UROLOGY SURGICAL PACK Used by medical... | Recall initiated due to inadequate validation/qualification of sterilization ... | Class II |
| Jan 7, 2016 | Catalog Number: 9002766 SHOULDER PACK Used by medical staff to perform sur... | Recall initiated due to inadequate validation/qualification of sterilization ... | Class II |
| Jan 7, 2016 | Catalog Number: 9002829 BASIC SURG PACK Used by medical staff to perform ... | Recall initiated due to inadequate validation/qualification of sterilization ... | Class II |
| Jan 7, 2016 | Catalog Number: 900080 CYSTOSCOPY SURGICAL PACK Used by medical staff to pe... | Recall initiated due to inadequate validation/qualification of sterilization ... | Class II |
| Jan 7, 2016 | Catalog Number: 9001062 ARTHROSCOPY SURGICAL PACK Used by medical staff to... | Recall initiated due to inadequate validation/qualification of sterilization ... | Class II |
| Jan 7, 2016 | Catalog Number: 9001966 LIVER & PANCREAS SURGERY Used by medical staff to... | Recall initiated due to inadequate validation/qualification of sterilization ... | Class II |
| Jan 7, 2016 | Catalog Number: 9002123 KNEE ARTHROSCOPY SURGICAL PACK Used by medical st... | Recall initiated due to inadequate validation/qualification of sterilization ... | Class II |
| Jan 7, 2016 | Catalog Number: 900998 CESAREAN SECTION SURGICAL PACK Used by medical sta... | Recall initiated due to inadequate validation/qualification of sterilization ... | Class II |
| Jan 7, 2016 | Catalog Number: 9001496 D&C LAPAROSCOPY SURGICAL PACK Used by medical staf... | Recall initiated due to inadequate validation/qualification of sterilization ... | Class II |
| Jan 7, 2016 | Catalog Number: 900474 LAPAROSCOPY SURGICAL PACK Used by medical staff to ... | Recall initiated due to inadequate validation/qualification of sterilization ... | Class II |
| Jan 7, 2016 | Catalog Number: 900052 MINOR PROCEDURE SURGICAL PACK Used by medical staff... | Recall initiated due to inadequate validation/qualification of sterilization ... | Class II |
| Jan 7, 2016 | Catalog Number: 9001300 NEURO-SPINE SURGICAL PACK Used by medical staff t... | Recall initiated due to inadequate validation/qualification of sterilization ... | Class II |
| Jan 7, 2016 | Catalog Number: 9001765 MINOR LACERATION TRAY Used by medical staff to per... | Recall initiated due to inadequate validation/qualification of sterilization ... | Class II |
| Jan 7, 2016 | Catalog Number: 900521 SURGICAL GOWN SMS POLY-REINFORCED, RAGLAN SLEEVE, AA... | Recall initiated due to inadequate validation/qualification of sterilization ... | Class II |
| Jan 7, 2016 | Catalog Number: 900281A LAPAROTOMY PACK Used by medical staff to perform s... | Recall initiated due to inadequate validation/qualification of sterilization ... | 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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