PlainRecalls

Resource Optimization & Innovation Llc

Compiled from official public sources by the editorial team.

228 recalls on record · Latest: Apr 27, 2022

Resource Optimization & Innovation Llc Recall Insight

Resource Optimization & Innovation Llc appears on 228 federal recall records indexed by PlainRecalls, out of 101,704 total recalls tracked across the FDA, CPSC, and NHTSA. That represents approximately 0.224% of the federal archive, a data point that is only interpretable alongside production volume, product mix, and decades of operation, because a high recall count alone does not establish fault. Large, diversified firms that sell tens of millions of units across many categories will mechanically accumulate more recall records than small manufacturers, even when their defect rates per unit shipped are comparable or lower. The most recent action on this firm is dated Apr 27, 2022, which is the anchor point for assessing whether enforcement is currently active or historical.

On this page of 50 entries, severity tagging shows 0 critical, 50 moderate, and 0 lower-severity recalls. Affected-unit counts are disclosed on 50 of 50 entries, unit-count disclosure is more common on CPSC and NHTSA actions and less common on FDA drug/device recalls, where lot numbers and distribution scope substitute for absolute totals. The records on this page span 1 distinct product categories, with issuing agencies dominated by FDA Devices (50). The date window on this page runs from Apr 5, 2017 to Apr 5, 2017.

Manufacturer-level browsing is useful when monitoring a single firm for patterns, whether recalls cluster around one product family (suggesting a specific design or supplier issue) or scatter across the firm's entire catalog (which can indicate systemic quality-control problems or deliberate regulator attention). Clicking into each recall reveals the specific hazard, remedy, and distribution scope that together determine whether a consumer is actually at risk. For decisions that depend on being current, deciding whether a product in your home is safe, whether to return a gift, or whether to accept a replacement, always verify the recall number on the issuing agency's site, because federal agencies amend, terminate, and re-scope recalls over time and only the agency's live record reflects the current legal status. This page aggregates what agencies have published publicly and is intended for consumer awareness and research.

FDA Devices Moderate Apr 5, 2017

Regard, Item Number: 800528004, Sterile, GS0612D - Lap Chole Pk - Westover Hills

FDA Devices Moderate Apr 5, 2017

Regard, Item Number: 800401002, Sterile, GS0470B - Lap PK - Spohn

FDA Devices Moderate Apr 5, 2017

Regard, Item Number: 800559003, Sterile, ET0648C - Head & Neck - Childrens Santa Rosa

FDA Devices Moderate Apr 5, 2017

Regard, Item Number: 800430004, Sterile, LD0499D - C Section Pk - Cabrini

FDA Devices Moderate Apr 5, 2017

Regard, Item Number: 880327009, Sterile, CV0758I - Open Heart A&B - OSU

FDA Devices Moderate Apr 5, 2017

Regard, Item Number: 800557002, Sterile, LD0646B - C Section - Childrens Santa Rosa

FDA Devices Moderate Apr 5, 2017

Regard, Item Number: 800418002, Sterile, GY0487B - Major Vaginal Pk - Spohn

FDA Devices Moderate Apr 5, 2017

Regard, Item Number: 800091003, Sterile, LD0692C - C Section - FMOL Lady of Angels

FDA Devices Moderate Apr 5, 2017

Regard, Item Number: 800407003, Sterile, OR0476C - Ortho Pk - Spohn

FDA Devices Moderate Apr 5, 2017

Regard, Item Number: 880327008, Sterile, CV0758H - Open Heart A&B - OSU

FDA Devices Moderate Apr 5, 2017

Regard, Item Number: 880341001, Sterile, GS0775A - Laparoscopic - OSU

FDA Devices Moderate Apr 5, 2017

Regard, Item Number: 800508004, Sterile, LD0586D - C Section - Jasper

FDA Devices Moderate Apr 5, 2017

Regard, Item Number: 800413004, Sterile, CV0482D- Vascular PK - Spohn

FDA Devices Moderate Apr 5, 2017

Regard, Item Number: 800413003, Sterile, CV0482C - Vascular PK - Spohn

FDA Devices Moderate Apr 5, 2017

Regard, Item Number: 800527003 Sterile, OR0611C - Hip Shoulder PK - Westover Hills

FDA Devices Moderate Apr 5, 2017

Regard, Item Number: 800525001, Sterile, OR0609A - Extremity Pack - Westover Hills

FDA Devices Moderate Apr 5, 2017

Regard, Item Number: 800555002, Sterile, HT0644B - Pediatric Card Cath - Childrens Santa Rosa

FDA Devices Moderate Apr 5, 2017

Regard, Item Number: 800526002 Sterile, ET0610B - Head and Neck - Westover Hills

FDA Devices Moderate Apr 5, 2017

Regard, Item Number: 800559002, Sterile, ET0648B - Head & Neck - Childrens Santa Rosa

FDA Devices Moderate Apr 5, 2017

Regard, Item Number: 800551003, Sterile, GS0640C - Lap Chole - Medical Center Santa Rosa

FDA Devices Moderate Apr 5, 2017

Regard, Item Number: 800546002, Sterile, GS0635B - Abdominal - Medical Center Santa Rosa

FDA Devices Moderate Apr 5, 2017

Regard, Item Number: 800508003, Sterile, LD0586C - C Section - Jasper

FDA Devices Moderate Apr 5, 2017

Regard, Item Number: 800407004, Sterile, OR0476D - Ortho PK - Spohn

FDA Devices Moderate Apr 5, 2017

Regard, Item Number: 800417001, Sterile, GY0486A - Laparoscopy Pk - Spohn

FDA Devices Moderate Apr 5, 2017

Regard, Item Number: 800401001, Sterile, GS0470A - Lap PK - Spohn

FDA Devices Moderate Apr 5, 2017

Regard, Item Number: 800422002, Sterile, OR0491B - Arthroscopy PK - Spohn

FDA Devices Moderate Apr 5, 2017

Regard, Item Number: 800425, Sterile, CV0494 - Av Access PK - Spohn

FDA Devices Moderate Apr 5, 2017

Regard, Item Number: 800416001, Sterile, GY0485A - Robotic Hysterectomy Pk - Spohn

FDA Devices Moderate Apr 5, 2017

Regard, Item Number: 800408004, Sterile, LD0477D - C-Section PK - Spohn

FDA Devices Moderate Apr 5, 2017

Regard, Item Number: 800535002 Sterile, LD0620B - C Section - New Braunfels

FDA Devices Moderate Apr 5, 2017

Regard, Item Number: 800422004, Sterile, OR0491D - Arthroscopy Pk - Spohn

FDA Devices Moderate Apr 5, 2017

Regard, Item Number: 800548002, Sterile, OR0637B - Extremity - Medical Center Santa Rosa

FDA Devices Moderate Apr 5, 2017

Regard, Item Number: 800553002, Sterile, OR0642B - Total Knee - Medical Center Santa Rosa

FDA Devices Moderate Apr 5, 2017

Regard, Item Number: 880327006, Sterile, CV0758F - Open Heart A&B - OSU

FDA Devices Moderate Apr 5, 2017

Regard, Item Number: 800411002, Sterile, NU0480B- Neuro PK - Spohn

FDA Devices Moderate Apr 5, 2017

Regard, Item Number: 800409003, Sterile, GS0478B - Lap Chole PK - Spohn

FDA Devices Moderate Apr 5, 2017

Regard, Item Number: 800550002, Sterile, OR0639B - Hip Shoulder - Medical Center Santa Rosa

FDA Devices Moderate Apr 5, 2017

Regard, Item Number: 800558002, Sterile, OR0647B - Extremity - Childrens Santa Rosa

FDA Devices Moderate Apr 5, 2017

Regard, Item Number: 880330005, Sterile, OR0761E - Total Hip - OSU

FDA Devices Moderate Apr 5, 2017

Regard, Item Number: 800508001, Sterile, LD0586A - C Section - Jasper

FDA Devices Moderate Apr 5, 2017

Regard, Item Number: 800410005, Sterile, CV0479E- Open Heart PK - Spohn

FDA Devices Moderate Apr 5, 2017

Regard, Item Number: 880327007, Sterile, CV0758G - Open Heart A&B - OSU

FDA Devices Moderate Apr 5, 2017

Regard, Item Number: 880330003, Sterile, OR0761C - Total Hip - OSU

FDA Devices Moderate Apr 5, 2017

Regard, Item Number: 800569003, Sterile, CV0659C - Open Heart A&B - Medical Center Santa Rosa

FDA Devices Moderate Apr 5, 2017

Regard, Item Number: 800525002 Sterile, OR0609B - Extremity Pack - Westover Hills

FDA Devices Moderate Apr 5, 2017

Regard, Item Number: 800409002, Sterile, GS0478B - Lap Chole PK - Spohn

FDA Devices Moderate Apr 5, 2017

Regard, Item Number: 800425002, Sterile, CV0494B - AV Access Pk - Spohn

FDA Devices Moderate Apr 5, 2017

Regard, Item Number: 800418001, Sterile, GY0487A - Major Vaginal PK - Spohn

FDA Devices Moderate Apr 5, 2017

Regard, Item Number: 800549002, Sterile, ET0638B - Head & Neck - Medical Center Santa Rosa

FDA Devices Moderate Apr 5, 2017

Regard, Item Number: 800508002, Sterile, LD0586B - C Section - Jasper

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Data Sources

  • Source: FDA + CPSC + NHTSA - federal recall filings naming this firm. Verify with FDA, CPSC, or NHTSA directly.
  • Source: PlainRecalls Manufacturer Index - firm-level aggregation across all three federal recall feeds

Every figure on PlainRecalls is rendered directly from official FDA, CPSC and NHTSA recall records, no number is typed in by an editor. Recalls are aggregated across FDA, CPSC and NHTSA filings that name this firm; the total reflects the federal record, not an independent investigation. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error. Data current as of July 2026.