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 12 critical, 36 moderate, and 2 lower-severity recalls. The page references 25 distinct recalling firms operating in 7 distinct product categories, with 43 of 50 records disclosing affected-unit counts. Issuing-agency distribution on this slice leans toward FDA Devices (29), NHTSA (7), CPSC (6), 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 Oct 10, 2018

CE18HKST CONT EPID 20G SOFTIP, Material Number 332084 Connection device used by physicians to provide various anesthetic and fluid administration devices with a single, common access point to a catheter for delivery of anesthetics. The connector is used in conjunction with the catheter for continuous administration of anesthetic fluids.

B. Braun Medical, Inc.

FDA Devices Moderate Oct 10, 2018

Capnostream20 N W/PRINTER CYVITAL, CS08798

Oridion Medical 1987 Ltd.

FDA Devices Moderate Oct 10, 2018

ES1827K SPINAL/EPIDURAL TRAY (LF), Material Number 333192 Connection device used by physicians to provide various anesthetic and fluid administration devices with a single, common access point to a catheter for delivery of anesthetics. The connector is used in conjunction with the catheter for continuous administration of anesthetic fluids.

B. Braun Medical, Inc.

FDA Devices Moderate Oct 10, 2018

ES1827KDS SPINAL/EPIDURAL FULL KIT, Material Number 333194 Connection device used by physicians to provide various anesthetic and fluid administration devices with a single, common access point to a catheter for delivery of anesthetics. The connector is used in conjunction with the catheter for continuous administration of anesthetic fluids.

B. Braun Medical, Inc.

FDA Devices Moderate Oct 10, 2018

CAPNOSTREAM 20P (US) N, Part Number CS08651-01

Oridion Medical 1987 Ltd.

FDA Devices Moderate Oct 10, 2018

CE18TKO PERIFIX ONE EPIDURAL FULL TRAY, Material Number 332282 Connection device used by physicians to provide various anesthetic and fluid administration devices with a single, common access point to a catheter for delivery of anesthetics. The connector is used in conjunction with the catheter for continuous administration of anesthetic fluids.

B. Braun Medical, Inc.

FDA Devices Moderate Oct 10, 2018

CE17TK CONT EPIDURALTUOHY, Material Number 332221 Connection device used by physicians to provide various anesthetic and fluid administration devices with a single, common access point to a catheter for delivery of anesthetics. The connector is used in conjunction with the catheter for continuous administration of anesthetic fluids.

B. Braun Medical, Inc.

FDA Devices Moderate Oct 10, 2018

CAPNOSTREAM 20P (COV-INTL) N W/PRINTER ROHS, CS051COV

Oridion Medical 1987 Ltd.

FDA Devices Moderate Oct 10, 2018

CAPNOSTREAM 20P (INTL) N - ROHS, Part Number CS08652-02

Oridion Medical 1987 Ltd.

FDA Devices Moderate Oct 10, 2018

Capnostream20 M W/PRINTER CYVITAL, CS08796

Oridion Medical 1987 Ltd.

FDA Devices Moderate Oct 10, 2018

Heart Ware(TM) HVAD(TM) System Controller/Controller Kits, Model Numbers: 1403, 1407, and 1420 Product Usage: The HeartWare HVAD System is indicated for hemodynamic support in patients with advanced, refractory left ventricular heart failure; either as a Bridge to Cardiac Transplantation (BTT), myocardial recovery, or as Destination Therapy (DT) in patients for whom subsequent transplantation is not planned.

Heartware, Inc.

FDA Devices Moderate Oct 10, 2018

CNB400TU3KUE 18GX4 CONTI THY ULTRA 360, Material Number 332170 Connection device used by physicians to provide various anesthetic and fluid administration devices with a single, common access point to a catheter for delivery of anesthetics. The connector is used in conjunction with the catheter for continuous administration of anesthetic fluids.

B. Braun Medical, Inc.

FDA Devices Critical Oct 10, 2018

ENDOLOGIX AFX/AFX2, Limb (Iliac) Extension Endograft, Rx Only, Sterile EO, AFX Limb Accessory Model #/REF: I16-16/C55, I16-16/C55F, I16-16/C88, I20-13/C70F, I20-13/C88F, I16-16/C55, I16-16/C55F, I16-16/C88, I20-13/C70F, I20-13/C88F; AFX Stand Alone I16-16/C55 SA, I16-16/C55F SA, I16-16/C88 SA, I20-13/C70F SA, I20-13/C88F SA, I20-20/C55 SA, I20-20/C55F SA, IS20-2

Endologix

FDA Devices Moderate Oct 10, 2018

CE17TKFSA FULL TRAY W/17G TUOHY 19G SPRW, Material Number 332080 Connection device used by physicians to provide various anesthetic and fluid administration devices with a single, common access point to a catheter for delivery of anesthetics. The connector is used in conjunction with the catheter for continuous administration of anesthetic fluids.

B. Braun Medical, Inc.

FDA Devices Moderate Oct 10, 2018

Capnostream20 (INTL) M W/PRINTER, CS08660

Oridion Medical 1987 Ltd.

FDA Devices Moderate Oct 10, 2018

CE18TOD CONT EPIDURAL TRAY LF, Material Number 332236 Connection device used by physicians to provide various anesthetic and fluid administration devices with a single, common access point to a catheter for delivery of anesthetics. The connector is used in conjunction with the catheter for continuous administration of anesthetic fluids.

B. Braun Medical, Inc.

FDA Devices Moderate Oct 10, 2018

CLAMP STYLE CATH. CONNECTOR 18-19 GA- LF, Material Number 332285 Connection device used by physicians to provide various anesthetic and fluid administration devices with a single, common access point to a catheter for delivery of anesthetics. The connector is used in conjunction with the catheter for continuous administration of anesthetic fluids.

B. Braun Medical, Inc.

FDA Devices Moderate Oct 10, 2018

Bronchovidescope BF-1T240

Olympus Corporation of the Americas

FDA Devices Moderate Oct 10, 2018

Capnostream20 (US) M W/PRINTER, Part Number CS08659

Oridion Medical 1987 Ltd.

FDA Devices Moderate Oct 10, 2018

Bronchovideoscope BF-P160

Olympus Corporation of the Americas

FDA Devices Moderate Oct 10, 2018

CAPNOSTREAM 20P (US) N - ROHS, Part Number CS08651-02

Oridion Medical 1987 Ltd.

FDA Devices Moderate Oct 10, 2018

CE17TOD CONT EPIDURAL TRAY LF, Material Number 332235 Connection device used by physicians to provide various anesthetic and fluid administration devices with a single, common access point to a catheter for delivery of anesthetics. The connector is used in conjunction with the catheter for continuous administration of anesthetic fluids.

B. Braun Medical, Inc.

FDA Devices Moderate Oct 10, 2018

CE17TKFPS PERIFIX FX CONT. EPID TRAY-LF, Material Number 332087 Connection device used by physicians to provide various anesthetic and fluid administration devices with a single, common access point to a catheter for delivery of anesthetics. The connector is used in conjunction with the catheter for continuous administration of anesthetic fluids.

B. Braun Medical, Inc.

FDA Devices Moderate Oct 10, 2018

GOVCE18TK ACCU-BLOC PERIFIX KIT, Material Number 332600 Connection device used by physicians to provide various anesthetic and fluid administration devices with a single, common access point to a catheter for delivery of anesthetics. The connector is used in conjunction with the catheter for continuous administration of anesthetic fluids.

B. Braun Medical, Inc.

FDA Devices Moderate Oct 10, 2018

CE17TKFMHDT 17 GA X 4 FULL EPID KIT, Material Number 332096 Connection device used by physicians to provide various anesthetic and fluid administration devices with a single, common access point to a catheter for delivery of anesthetics. The connector is used in conjunction with the catheter for continuous administration of anesthetic fluids.

B. Braun Medical, Inc.

FDA Devices Moderate Oct 10, 2018

Bronchovideoscope BF-3C160

Olympus Corporation of the Americas

FDA Devices Moderate Oct 10, 2018

CE17TB19C CONT EPIDURAL TRAY, Material Number 332242 Connection device used by physicians to provide various anesthetic and fluid administration devices with a single, common access point to a catheter for delivery of anesthetics. The connector is used in conjunction with the catheter for continuous administration of anesthetic fluids.

B. Braun Medical, Inc.

FDA Devices Moderate Oct 10, 2018

CAPNOSTREAM 20 (US) N, Part Number CS08651

Oridion Medical 1987 Ltd.

FDA Devices Moderate Oct 10, 2018

Leica Biosystems HistoCore SPECTRA ST, Slide Stainer, Automated Product Usage: The intended use of this device is a stainer for laboratory applications and intended for the preparation of histological and cytological specimens.

Leica Microsystems, Inc.

CPSC No agency class Oct 10, 2018

Briggs & Stratton Recalls Portable Generator Fuel Tank Replacement Caps, Due to Fire Hazard

Kelch, of Sheboygan Falls, Wis., a division of Bemis Manufacturing Company

CPSC No agency class Oct 10, 2018

Canyon Recalls Mountain Bikes Due to Crash Hazard (Recall Alert)

A&I Industries Ltd., of China

CPSC No agency class Oct 10, 2018

Spiraledge Recalls Yoga Backless Chairs Due to Fall Hazard (Recall Alert)

Zhangzhou Zhonghao Furniture Co., Ltd. of Fujian, China

USDA FSIS Critical Oct 10, 2018

Malone's Fine Sausage, Inc. Recalls Pork Head Cheese Products due to Possible Listeria Contamination

Malone's Fine Sausage, Inc.

CPSC No agency class Oct 9, 2018

Cracker Barrel Old Country Store Recalls Decorative Pineapples Due to Laceration Hazard

CBOCS Distribution Inc., dba Cracker Barrel Old Country Store, of Lebanon, Tenn.

CPSC No agency class Oct 9, 2018

Marker Recalls Kingpin Ski Bindings Due to Fall Hazard

Marker CZ, of Czech Republic

NHTSA No agency class Oct 5, 2018

HYUNDAI 2017-2018: HYBRID PROPULSION SYSTEM: INVERTER

HYUNDAI

NHTSA No agency class Oct 5, 2018

FREIGHTLINER,WESTERN STAR 2018-2019: SERVICE BRAKES, AIR:DISC:CALIPER

FREIGHTLINER,WESTERN STAR

NHTSA No agency class Oct 5, 2018

FREIGHTLINER,WESTERN STAR 2019: STEERING

FREIGHTLINER,WESTERN STAR

NHTSA No agency class Oct 5, 2018

INTERNATIONAL 2018-2019: EXTERIOR LIGHTING:HEADLIGHTS

INTERNATIONAL

USDA FSIS Critical Oct 5, 2018

Canteen/Covenco Recalls Ready-To-Eat Breaded Chicken Products Due to Misbranding and Undeclared Allergens

Compass Group/Canteen

USDA FSIS Critical Oct 5, 2018

Ukrop's Homestyle Foods Recalls Ready-To-Eat Meat and Poultry Products Due to Possible Listeria Contamination

Ukrop's Homestyle Foods

CPSC No agency class Oct 4, 2018

Metal Playground Climbers Recalled by BCI Burke Due to Strangulation Hazard (Recall Alert)

BCI Burke Company, of Fond du Lac, Wis.

NHTSA No agency class Oct 4, 2018

SUZUKI 2017-2018: FUEL SYSTEM, GASOLINE:DELIVERY:FUEL PUMP

SUZUKI

NHTSA No agency class Oct 4, 2018

TOYOTA 2018-2019: ELECTRICAL SYSTEM:SOFTWARE

TOYOTA

NHTSA No agency class Oct 4, 2018

TOYOTA 2010-2014: HYBRID PROPULSION SYSTEM

TOYOTA

USDA FSIS Critical Oct 4, 2018

JBS Tolleson, Inc. Recalls Raw Beef Products Due to Possible Salmonella Newport Contamination

JBS Tolleson Inc.

FDA Food Low Oct 3, 2018

TRADER JOE'S Cinnamon Coffee Cake; NET WT. 16 OZ (1 LB) 454g; SKU# 94235; UPC: 00942355

Pin Hsiao & Associates, LLC dba Zen Bakery

FDA Food Moderate Oct 3, 2018

Gotham Greens Classic Pesto 6.5 oz. plastic cup, 12 cups per case. Refrigerated. UPC 85392700334

Brett Anthony Foods

FDA Food Moderate Oct 3, 2018

Swanson Ultra, Himalayan Crystal Salt, #SWU403, Net Wt. 35.27 oz. (2.2 lbs) (1,000 grams). Product of Pakistan. Distributed by Swanson Health Products, Fargo, ND 58104.

Swanson Health Products, Inc

FDA Food Low Oct 3, 2018

Caffeine-Free Barq s Root Beer 12 Pack, 12 oz cans

Swire Coca Cola USA

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.