PlainRecalls

2018 Recall Year Insight

Federal agencies issued 7,928 product recalls indexed by PlainRecalls in calendar year 2018. That represents about 7.59% of the 104,423 total recalls we track from 1995 through the present, and averages roughly 21.7 recalls per day across the FDA, CPSC, USDA FSIS, and NHTSA combined. Year-level views are the cleanest way to see macro patterns: volume spikes often correlate with new regulatory priorities (e.g., infant-sleep products after 2021, lithium-ion batteries after 2022), supply-chain contamination events, or changes in agency enforcement intensity, while quiet years can reflect either genuine product-safety improvements or reduced agency staffing and reporting lag. With 159 pages at 50 recalls each, browsing this year end-to-end gives a statistically representative sample of what the federal recall pipeline looked like in 2018.

On this page of 50 records, severity classification shows 8 critical, 33 moderate, and 9 lower-severity recalls. The page references 29 distinct recalling firms operating in 9 distinct product categories, with 47 of 50 records disclosing affected-unit counts. Issuing-agency distribution on this slice leans toward FDA Food (18), FDA Devices (16), CPSC (8), which matters because each agency's recall authority, hazard framing, and remedy mechanism differ, an FDA food recall, a CPSC consumer-product recall, and a NHTSA vehicle recall are legally distinct instruments even when the underlying hazard language sounds similar. Reviewing the dominant agency for a given year is one of the fastest ways to understand where federal attention was concentrated.

Year-indexed browsing serves three practical purposes: historical research (tracking how a hazard class evolved over time), consumer action (finding whether a product purchased in 2018 was later recalled), and journalistic or regulatory context (understanding what the enforcement landscape looked like in a given period). Every record on this page links to a full detail view with the hazard, remedy, distribution, and agency-assigned recall number, always use that recall number to verify current status directly with the issuing agency before acting on time-sensitive remedies, because agencies amend, terminate, and expand recalls in the months and years after initial publication. Data on this page reflects federal agency public filings; the agency's live record remains authoritative for legal, medical, or safety decisions. Verify with FDA openFDA, CPSC, USDA FSIS, or NHTSA for the system-of-record on any specific recall. PlainRecalls indexes this archive for research and consumer awareness purposes.

FDA Devices Moderate Mar 21, 2018

CR-FLEX GSF PRECOAT SZ C-L¿ CR-FLEX GSF PRECOAT SZ C-R¿ CR-FLEX GSF PRECOAT SZ D-L¿ CR-FLEX GSF PRECOAT SZ D-R¿ CR-FLEX GSF PRECOAT SZ E-L¿ CR-FLEX GSF PRECOAT SZ E-R¿ CR-FLEX GSF PRECOAT SZ F-L¿ CR-FLEX GSF PRECOAT SZ F-R¿ CR-FLEX GSF PRECOAT SZ G-L¿ CR-FLEX GSK PRECOAT SZ G-R¿ " These devices are indicated for patients with: - Painful and/or disabling knee joints due to osteoarthritis or traumatic arthritis. - Previous tibial condyle or plateau fractures with loss of anatomy or fun

Zimmer Biomet, Inc.

FDA Devices Moderate Mar 21, 2018

Trabecular Metal¿ Primary Hip Prosthesis; Part Numbers: 1. 00-7864-013-00 (UDI: (01) 00889024139251 (17) 250731 (10) 63703649), and 2. 00-7864-013-20 (UDI: (01) 00889024139268 (17) 250731 (10) 63703681)

Zimmer Biomet, Inc.

FDA Devices Moderate Mar 21, 2018

CPT 12/14 COCR SIZE 1 EXT prosthesis, hip, semi-constrained, metal/polymer, porous uncemented

Zimmer Biomet, Inc.

FDA Devices Moderate Mar 21, 2018

Difco" Agar Noble, 500g bottle Noble Agar is a solidifying agent that is essentially free of impurities. It is used in electrophoretic and nutritional procedures and in preparing microbiological culture media when increased purity is required.

Becton Dickinson & Co.

FDA Devices Moderate Mar 21, 2018

Proteus 235, Proton Therapy System a medical device designed to produce and delivers a proton beam for the treatment of patients with localized tumors and other conditions susceptible to treatment by radiation.

Ion Beam Applications S.A.

FDA Devices Low Mar 21, 2018

Immunoassay Premium Plus Controls (3x4x5mL and 12x5mL packages)

Randox Laboratories

FDA Devices Moderate Mar 21, 2018

Newton Wire Guide

Cook Inc.

FDA Devices Moderate Mar 21, 2018

Alden HP59 Sphere Daily Wear Soft contact; Catalog Number: AOHPS59 Product Usage: The ALDEN SPHERE LENS for daily wear is indicated for the correction of visual acuity in aphakic and not aphakic persons with non-diseased eyes with refractive ametropia (myopia or hyperopia). The lens may be worn by persons who exhibit refractive astigmatism of 1.50 diopters or less where the astigmatism does not interfere with visual acuity.

Alden Optical

FDA Devices Moderate Mar 21, 2018

AGB+ Pressure Injectable Multi- Lumen CVC Kit Product Usage: The Arrow¿ CVC is indicated to provide short-term (< 30 days) central venous access for treatment of diseases or conditions requiring central venous access including, but not limited to: multiple infusions of fluids, medications, or chemotherapy infusion of fluids that are hypertonic, hyperosmolar, or have divergent pH values frequent blood sampling or blood/blood component infusions infusion of incompatible medications

Arrow International Inc

FDA Devices Moderate Mar 21, 2018

Proteus 235, Uniform and Pencil Beam Scanning The Proton Therapy System - Proteus 235 (brand names: Proteus Plus and Proteus ONE) is a medical device designed to produce and deliver a proton beam for the treatment of patients with localized tumors and other conditions susceptible to treatment by radiation. The PTS may include a fixed small beam treatment room dedicated to the treatment of patients with localized tumors and other conditions susceptible to treatment by radiation localized to th

Ion Beam Applications S.A.

FDA Devices Moderate Mar 21, 2018

GENDER SOLUTIONS NATURAL-KNEE FLEX SYSTEM GENDER SOLUTIONS FEMALE (GSF) FEMORAL COMPONENT NONPOROUS¿ N-K FLX GSF NP FEM SZ 0 RT N-K FLX GSF NP FEM SZ 4 LT N-K FLX GSF NP FEM SZ 4 RT Components with CSTi porous coating are indicated for uncemented or cemented use in skeletally mature individuals with intact medial and lateral collateral ligaments undergoing primary surgery for rehabilitating knees damaged as a result of Noninflammatory Degenerative Joint Disease (NIDJD) or Inflam

Zimmer Biomet, Inc.

FDA Devices Moderate Mar 21, 2018

DELTA CER FEM HD 32/0MM T1 Product Usage: For use in hip arthroplasty

Zimmer Biomet, Inc.

FDA Devices Moderate Mar 21, 2018

VERSYS 6 INCH BEADED FC STEM 12X160MM LM 13X160MM LM 15X160MM LM 17X160MM LM Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented

Zimmer Biomet, Inc.

FDA Devices Moderate Mar 21, 2018

The GLOBAL UNITE Platform Shoulder System is intended for cemented or uncemented total shoulder or hemi-shoulder replacement procedures, Product labeling: LE¿O-1100-30-000 REV D.pdf.pdf, LE¿O-1100-40-000 REV D.pdf.pdf, LE¿O-110030100_REV D.pdf.pdf, LE¿O-110030110_REV D.pdf.pdf, LE¿O-110030120_REV D.pdf.pdf

DePuy Orthopaedics, Inc.

FDA Devices Moderate Mar 21, 2018

ASTERA Multifocal Toric Daily Wear Soft contact; Catalog Number: AOAMT54 Product Usage: The ALDEN TORIC LENS for daily wear is indicated for the correction of visual acuity in aphakic and not aphakic persons with non-diseased eyes with refractive ametropia (myopia or hyperopia) and/or possesses refractive astigmatism not exceeding 10 Diopters.

Alden Optical

FDA Devices Moderate Mar 21, 2018

Pressure Injectable Multi- Lumen Central Venous Catheterization Kit with Blue FlexTip(R), ARROWg+ard Blue PLUS(R) Product Usage: The Arrow¿ CVC is indicated to provide short-term (< 30 days) central venous access for treatment of diseases or conditions requiring central venous access including, but not limited to:  multiple infusions of fluids, medications, or chemotherapy  infusion of fluids that are hypertonic, hyperosmolar, or have  divergent pH values  frequent blood sampling or bloo

Arrow International Inc

CPSC No agency class Mar 21, 2018

Kidde Recalls Dual Sensor Smoke Alarms Due to Risk of Failure to Alert Consumers to a Fire

Fyrnetics Limited, of Hong Kong

NHTSA No agency class Mar 21, 2018

BMW 2012-2018: EQUIPMENT

BMW

USDA FSIS Critical Mar 21, 2018

California Jerky Factory, Inc. Recalls Beef Jerky Products Due to Possible Processing Deviation

California Jerky Factory, Inc.

CPSC No agency class Mar 20, 2018

Briggs & Stratton Recalls Riding Mowers Due to Risk of Injury

Briggs & Stratton Corp., of Wauwatosa, Wis.

USDA FSIS Critical Mar 20, 2018

Mickey Brown, Inc Recalls Beef Burrito Products Produced Without Benefit of Inspection

Mickey Brown, Inc.

CPSC No agency class Mar 19, 2018

Carrier® Recalls to Repair Commercial Rooftop HVAC Units Due to Fire Hazard (Recall Alert)

Carrier México, S.A. de C.V.

USDA FSIS Critical Mar 16, 2018

SMI Holdings, Inc Recalls Beef Products Due to Possible Salmonella Contamination

Stampede Culinary Partners, Inc.

CPSC No agency class Mar 15, 2018

Beanworthy Recalls Combination Battery Chargers/Hand Warmers Due to Fire and Burn Hazard; Sold Exclusively at Amazon.com (Recall Alert)

Shenzhen Olive Technology Co. LTD, of China

CPSC No agency class Mar 15, 2018

eheat Recalls Envi Wall Heaters Due to Overheating and Burn Hazard (Recall Alert)

eheat, Inc., of Tomball, Texas

CPSC No agency class Mar 15, 2018

Handi-Craft Recalls Dr. Brown's Lovey Pacifier & Teether Holders Due to Choking Hazard

Yangzhou Rich Arts & Crafts Co., Ltd., of Yang Zhou City, China

CPSC No agency class Mar 15, 2018

Louis Garneau Recalls Bicycle Helmets Due to Risk of Head Injury

Strategic Sports Limited, of China

CPSC No agency class Mar 15, 2018

Southwire Recalls Wi-Fi Switches Due to Fire Hazard

Southwire Company, LLC, of Carrollton, Ga.

NHTSA No agency class Mar 15, 2018

MERCEDES-BENZ 2016-2018: STRUCTURE:BODY:ROOF AND PILLARS

MERCEDES-BENZ

NHTSA No agency class Mar 15, 2018

TOYOTA 2018: EQUIPMENT:OTHER:LABELS

TOYOTA

USDA FSIS Critical Mar 15, 2018

Johnsonville, LLC Recalls Smoked Pork Sausage Products due to Possible Foreign Matter Contamination

Johnsonville, LLC

USDA FSIS Critical Mar 15, 2018

Standard Meat Company Recalls Beef Products Due to Possible Salmonella Contamination

Standard Meat Company

FDA Food Moderate Mar 14, 2018

Grape Fanta, Grape Flavored Soda, 12 oz (355 mL) cans, packed in 12 packs, Canned under the authority of the Coca-Cola Company, Atlanta, GA

Heartland Coca-Cola Bottling Company

FDA Food Moderate Mar 14, 2018

Pibb Zero, Artificially Flavored Sugar Free Spicy Cherry Soda 12 oz (355 mL) cans, packed in 12 packs, Canned under the authority of the Coca-Cola Company, Atlanta, GA

Heartland Coca-Cola Bottling Company

FDA Food Low Mar 14, 2018

Springside Monterey Jack Caribbean Red Hot Cheese Packaged in the following sizes: Net Wt. 1 lb. and 40 lbs.

Springside Cheese Corp

FDA Food Moderate Mar 14, 2018

Diet Coke Lime, 12 oz (355 mL) cans, packed in 12 packs, Canned under the authority of the Coca-Cola Company, Atlanta, GA

Heartland Coca-Cola Bottling Company

FDA Food Low Mar 14, 2018

Springside Monterey Jack Cheese Packaged in the following sizes: Net Wt. 8 oz., 5 lb. and 40 lbs.

Springside Cheese Corp

FDA Food Moderate Mar 14, 2018

Cherry SKI LEMON ORANGE AUTHENTIC CITRUS SODA 12 oz can CONTAINS: CARBONATED WATER, HIGH FRUCTOSE CORN SYRUP, LEMON JUICE CONCENTRATE, ORANGE JUICE CONCENTRATE, CITRIC ACID, NATURAL FLAVOR, SODIUM BENZOATE (PRESERVATIVE), CAFFEINE, CELLULOSE GUM, RED #4, GUM ARABIC, BLUE #1. UPC: 0 71644 20103 0

Double-Cola Co.-USA dba The Double Cola Company

FDA Food Moderate Mar 14, 2018

Sprite Zero, Lemon-Lime Soda, Zero Calories, 12 oz (355 mL) cans, packed in 12 packs, Canned under the authority of the Coca-Cola Company, Atlanta, GA

Heartland Coca-Cola Bottling Company

FDA Food Low Mar 14, 2018

Springside Monterey Jack Chicken Soup Cheese Packaged in the following sizes: Net Wt. 1 lb. and 40 lbs.

Springside Cheese Corp

FDA Food Low Mar 14, 2018

Springside Monterey Jack Chipotle Cheese Packaged in the following sizes: Net Wt. 8 oz., 1 lb. and 40 lbs.

Springside Cheese Corp

FDA Food Low Mar 14, 2018

Springside Monterey Jack Morel & Leek Cheese Packaged in the following sizes: Net Wt. 8 oz., 1 lb. and 40 lbs.

Springside Cheese Corp

FDA Food Moderate Mar 14, 2018

Caffeine Free Coke Zero, 12 oz (355 mL) cans, packed in 12 and 24 packs, Canned under the authority of the Coca-Cola Company, Atlanta, GA

Heartland Coca-Cola Bottling Company

FDA Food Low Mar 14, 2018

Springside Monterey Jack Pueblo Cheese packaged in the following sizes: Net Wt. 8 oz., and 5 lbs.

Springside Cheese Corp

FDA Food Moderate Mar 14, 2018

BELCA Soy Sauce, Contenido Neto: Un Gal¿n (128 fl. oz), Distribuido por: Mister Price Inc. San Juan, P.R. 00936

Gasco Industrial, Corp.

FDA Food Low Mar 14, 2018

Springside Monterey Jack Garden Vegetable Cheese, 40 lbs.

Springside Cheese Corp

FDA Food Moderate Mar 14, 2018

Product packaged in the following ways A) Sonne's, No. 17, Natural Source Vitamin C, Dietary Supplement, (920 mg tablet wt.) Contents - 120 Tablets, National Distributors: Sonne's Organic Foods, Inc. N. Kansas City, MO 64116; B) Springreen, No. 87, Natural Source Vitamin C, Dietary Supplement, (920 mg tablet wt.) Contents - 120 Tablets, National Distributors: Springreen Products, Inc. N. Kansas City, MO 64116;

Vitalab Co Inc

FDA Food Moderate Mar 14, 2018

Dr Pepper Diet, 12 oz (355 mL) cans, packed in 12 and 24 packs, Canned under the authority of Dr Pepper Company, Plano, TX

Heartland Coca-Cola Bottling Company

FDA Food Low Mar 14, 2018

Springside Monterey Jack Onion & Chives Cheese Net Wt. 1 lb.

Springside Cheese Corp

FDA Food Moderate Mar 14, 2018

Coca-Cola, Vanilla Flavor, 12 oz (355 mL) cans, packed in 12 packs, Canned under the authority of the Coca-Cola Company, Atlanta, GA

Heartland Coca-Cola Bottling Company

Nearby Recall Years

Browse recalls from adjacent calendar years to see how federal enforcement volume has shifted over time.

Compare 2018 with 2017 →

Data Sources

  • Source: FDA openFDA Enforcement API - calendar-year recall filings for food, drugs, and devices
  • Source: USDA FSIS Recalls - calendar-year meat, poultry, and processed egg product recall filings
  • Source: CPSC + NHTSA - consumer product and vehicle recall feeds for 2018

Every figure on PlainRecalls is rendered directly from official FDA, CPSC, USDA FSIS and NHTSA recall records; no number is typed in by an editor. Figures cover calendar year 2018 across the FDA, CPSC, USDA FSIS and NHTSA federal recall feeds. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error. Data current as of September 2026.