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 9 critical, 39 moderate, and 2 lower-severity recalls. The page references 26 distinct recalling firms operating in 7 distinct product categories, with 41 of 50 records disclosing affected-unit counts. Issuing-agency distribution on this slice leans toward FDA Devices (34), NHTSA (5), FDA Food (5), 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 Jul 11, 2018

Zimmer¿ M/L Taper Hip Prosthesis With Kinectiv¿ Technology Cementless, Size 5; 00-7713-005-00

Zimmer Biomet, Inc.

FDA Devices Moderate Jul 11, 2018

microtargeting" Depth Stop Adapter, Product Model Number, Product Number 66-AC-DS(1.8),

FHC, Inc.

FDA Devices Low Jul 11, 2018

ECOLAB MICROTEK Rolled Probe Cover, 2.0 cm x 20 cm (.8 in x 8 in), Ref PC0905, packaged 1 probe cover/pouch, 25 pouches/carton, 2 cartons/shipping case, Sterile, RX. To be used as a physical barrier for protection against the effects of environmental exposure (e.g. body fluids, gels) and/or to maintain the required hygienic level of various diagnostic or surgical procedures which utilize a transducer (probe).

ECOLAB INC

FDA Devices Moderate Jul 11, 2018

microTargeting" Drive System, Product Number MT-DS-01

FHC, Inc.

FDA Devices Moderate Jul 11, 2018

LFIT Anatomic CoCr Femoral Heads, Catalog No. 6260-9-144

Howmedica Osteonics Corp.

FDA Devices Moderate Jul 11, 2018

microTargeting" STar" Drive System (Motorized) Distributed by Medtronic, Product Number FC8002

FHC, Inc.

FDA Devices Moderate Jul 11, 2018

26-Lead Transfer Set for use with APEX¿ Compounding System, Product Catalog Number 2112550

B. Braun Medical, Inc.

FDA Devices Moderate Jul 11, 2018

Zimmer¿ M/L Taper Hip Prosthesis With Kinective¿ Technology Cementless, Size 12.5; 00-7713-012-00

Zimmer Biomet, Inc.

FDA Devices Moderate Jul 11, 2018

Zimmer¿ M/L Taper Hip Prosthesis With Kinective¿ Technology Cementless, Size 15; 00-7713-015-00

Zimmer Biomet, Inc.

FDA Devices Moderate Jul 11, 2018

Zimmer¿ M/L Taper Hip Prosthesis With Kinective¿ Technology Cementless, Size 7.5; 00-7713-007-00

Zimmer Biomet, Inc.

FDA Devices Moderate Jul 11, 2018

microTargeting" Lead Adapter for microTargeting" Drive, Product Number 66-CN-DB

FHC, Inc.

FDA Devices Moderate Jul 11, 2018

Zimmer¿ M/L Taper Hip Prosthesis With Kinective¿ Technology Cementless, Size 17.5; 00-7713-017-00

Zimmer Biomet, Inc.

FDA Devices Moderate Jul 11, 2018

microTargeting" Drive System Distributed by Medtronic, Product Number 9033G0601

FHC, Inc.

FDA Devices Moderate Jul 11, 2018

LFIT Anatomic CoCr Femoral Heads, Catalog No. 6260-9-140

Howmedica Osteonics Corp.

FDA Devices Moderate Jul 11, 2018

Multi-Lumen Central Venous Catheterization Set with Blue FlexTip Catheter, CS-15853-E Product CVCs are intended to permit venous access to the central circulation through a single puncture site by way of the femoral, jugular, or subclavian veins.

Arrow International Inc

FDA Devices Moderate Jul 11, 2018

St. Jude Medical CONFIRM Rx Insertable Cardiac Monitor, Sterile EO, Model #: DM3500 The Confirm Rx ICM is indicated for the monitoring and diagnostic evaluation of patients who experience unexplained symptoms such as: dizziness, palpitations, chest pain, syncope, and shortness of breath, as well as patients who are at risk for cardiac arrhythmias. It is also indicated for patients who have been previously diagnosed with atrial fibrillation or who are susceptible to developing atrial fibrillat

St Jude Medical Inc.

FDA Devices Moderate Jul 11, 2018

microTargeting" STar" Drive System (Manual) Distributed by Medtronic, Product Number FC8001

FHC, Inc.

FDA Devices Moderate Jul 11, 2018

microTargeting" Lead Adapter for STar" Drive, Product Number 70-CN-DB

FHC, Inc.

FDA Devices Moderate Jul 11, 2018

Zimmer¿ M/L Taper Hip Prosthesis With Kinective¿ Technology Cementless, Size 9; 00-7713-009-00

Zimmer Biomet, Inc.

FDA Devices Moderate Jul 11, 2018

microTargeting" Drive System, Product Number 66-ZD-MD-01

FHC, Inc.

FDA Devices Moderate Jul 11, 2018

Merlin PCS Programmer Software: 3330 The Merlin PCS programmer (model 3650) is a portable, external device used to support the implanted device, and for this recall the software that resides on the programmer (software model 3330) is the method of delivery of the new firmware.

St Jude Medical Inc.

FDA Devices Moderate Jul 11, 2018

microTargeting" Drive System Distributed by Medtronic, Product Number FC1006

FHC, Inc.

FDA Devices Moderate Jul 11, 2018

Zimmer¿ M/L Taper Hip Prosthesis With Kinective¿ Technology Cementless, Size 11; 00-7713-011-00

Zimmer Biomet, Inc.

FDA Devices Moderate Jul 11, 2018

Angio-Seal Evolution Vascular Closure Device, Cat. No. C610135

Terumo Medical Corp

FDA Devices Moderate Jul 11, 2018

microTargeting" STar" Drive System (Motorized), Product Number 70-ZD-ME

FHC, Inc.

FDA Devices Moderate Jul 11, 2018

Cannulated Driver Handle, Catalog #: 210-00-003, Rx Only, Non Sterile

Trilliant Surgical Ltd.

FDA Devices Moderate Jul 11, 2018

LFIT Anatomic CoCr Femoral Heads, Catalog No. 6260-9-236

Howmedica Osteonics Corp.

FDA Devices Moderate Jul 11, 2018

Zimmer M/L Taper Hip Prosthesis Plasma Sprayed, Size 4 Extended Offset, 00-7711-004-40

Zimmer Biomet, Inc.

FDA Devices Moderate Jul 11, 2018

Zimmer¿ M/L Taper Hip Prosthesis With Kinective¿ Technology Cementless, Size 22.5; 00-7713-022-00

Zimmer Biomet, Inc.

FDA Devices Moderate Jul 11, 2018

microTargeting" STar" Drive System (Motorized), Product Number ST-DS-ME

FHC, Inc.

FDA Devices Moderate Jul 11, 2018

LFIT Anatomic CoCr Femoral Heads, Catalog No. 6260-9-136

Howmedica Osteonics Corp.

FDA Devices Moderate Jul 11, 2018

Vulcan Fast Red Chromogen Kit 2, part of an immunohistochemistry (IHC) procedure using an alkaline phosphatase (AP) detection system. Catalog numbers FR805-5L and FR805S

Biocare Medical, LLC

FDA Devices Moderate Jul 11, 2018

Zimmer¿ M/L Taper Hip Prosthesis With Kinective¿ Technology Cementless, Size 10; 00-7713-010-00

Zimmer Biomet, Inc.

FDA Devices Moderate Jul 11, 2018

VITROS Chemistry Products PHYT Slides, Catalog Number 8298671. in vitro diagnostic

Ortho-Clinical Diagnostics

CPSC No agency class Jul 11, 2018

Burton Recalls Snowboard Boots Due to Fall Hazard (Recall Alert)

Jia You Plastics, of China

NHTSA No agency class Jul 11, 2018

VOLKSWAGEN 2015-2018: STEERING:COLUMN LOCKING:ANTI-THEFT DEVICE

VOLKSWAGEN

CPSC No agency class Jul 10, 2018

ORTOVOX Recalls Avalanche Transceivers Due to Loss of Emergency Communications Capability

Ortovox, of Germany

NHTSA No agency class Jul 10, 2018

MERCEDES-BENZ 2017-2018: STRUCTURE:BODY

MERCEDES-BENZ

NHTSA No agency class Jul 10, 2018

SUBARU 2018: TIRES

SUBARU

USDA FSIS Critical Jul 9, 2018

Afandina Halal Recalls Raw Chicken Products Produced Without Benefit of Inspection

Afandina Halal

CPSC No agency class Jul 6, 2018

Camso Recalls Dirt to Snow Bike Conversion Kits Due to Crash and Impact Hazards

Camso Inc. of Quebec, Canada

CPSC No agency class Jul 6, 2018

Sandoz and Novartis Recall Prescription Drug Blister Packages Due to Failure to Meet Child-Resistant Closure Requirements

Sandoz Inc., of Princeton, N.J.

NHTSA No agency class Jul 6, 2018

BMW 2018-2019: SERVICE BRAKES, HYDRAULIC:FOUNDATION COMPONENTS:DISC:CALIPER

BMW

NHTSA No agency class Jul 6, 2018

NISSAN 2007-2008: AIR BAGS:FRONTAL:PASSENGER SIDE:INFLATOR MODULE

NISSAN

USDA FSIS Low Jul 6, 2018

Recall Notification Report 059-2018 (Beef Jerky Products)

Tillamook Country Smoker, LLC

FDA Food Critical Jul 4, 2018

Mini Chocolate Croissants, 8-Pack, packaged in a clear plastic clam-shell container, net wt. 7.6 oz., UPC 8 04600 10905 1

New Seasons Market LLC

FDA Food Moderate Jul 4, 2018

Meyer Lemon Chia Muffin, 4-pack, packaged in a clear clamshell container, net wt. 13.6 oz., UPC 8 40600 10953 2

New Seasons Market LLC

FDA Food Critical Jul 4, 2018

Utz Restaurant Style Tortilla Chips; Net Wt 17 oz; White Corn Tortilla Chips; UPC: 0-41780-00383-6; Exp. Date Jun 16 18; UTZ Quality Foods, Inc., Hanover, PA 17331; Utz Restaurant Style Tortilla Chips; Net Wt 11.5 oz; White Corn Tortilla Chips; UPC: 0-41780-00384-3; Exp date Jun 16 18; UTZ Quality Foods, Inc., Hanover, PA 17331; Weis Signature Collection; Restaurant Style White Corn Tortilla Chips; Net Wt 11 oz; Manufactured for Weis Markets, Sunbury, PA 17801; UPC: 0-41497-00426-3 E

Utz Quality Food Inc

FDA Food Moderate Jul 4, 2018

Blood & Internal Cleanser, Dietary Supplement

Nutreglo Products, LLC.

FDA Food Critical Jul 4, 2018

Al Reef dried apricot sour, 12 oz., packed in plastic, 24 packages per case

Golden Star Wholesale Inc

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.