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, 34 moderate, and 4 lower-severity recalls. The page references 29 distinct recalling firms operating in 8 distinct product categories, with 48 of 50 records disclosing affected-unit counts. Issuing-agency distribution on this slice leans toward FDA Devices (22), FDA Food (21), FDA Drug (3), 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.

CPSC No agency class Dec 13, 2018

Women's Scarves Recalled by Raj Imports Due to Violation of Federal Flammability Standard

NHTSA No agency class Dec 13, 2018

TOYOTA 2018-2019: SERVICE BRAKES, HYDRAULIC:FOUNDATION COMPONENTS:MASTER CYLINDER

TOYOTA

NHTSA No agency class Dec 13, 2018

LEXUS,TOYOTA 2008-2019: AIR BAGS:FRONTAL:PASSENGER SIDE:INFLATOR MODULE

LEXUS,TOYOTA

USDA FSIS Moderate Dec 13, 2018

Vermont Packinghouse, LLC Recalls Raw Intact Bone-In Beef Products due to Possible Specified Risk Materials Contamination

FDA Food Moderate Dec 12, 2018

TILLAMOOK COUNTY CREAMERY ASSOC

FDA Food Low Dec 12, 2018

NOW Vitamin B-50 Complex with C 100 Veg Caps

NOW Foods

FDA Food Moderate Dec 12, 2018

Tillamook Mudslide ice cream (item #63006), packaged in 3 gallon tub. UPC 0 72830 63006 1. The label is read in parts: "***TILLAMOOK MUDSLIDE ICE CREAM*** ALLERGEN INFORMATION: This product contains milk, peanut, soy, tree nut (coconut), egg. It is made with equipment that also makes product containing wheat.***"

TILLAMOOK COUNTY CREAMERY ASSOC

FDA Food Critical Dec 12, 2018

Green Cedar Ackawi cheese in small clear plastic shrink wrapped packaging bearing a sell by date of March 26, 2019 or later. The sell by date is on a white sticker on the back of the product. , Keep Refrigerated

Harb Dairy, Inc. DBA Green Cedar Dairy

FDA Food Moderate Dec 12, 2018

Smartypants Kids Complete, Non GMO Multi and omega 3's vitamin D3 for bones, vitamin B12 for Energy: 90 gummies. UPC 8 5136 00425 5 Distributed by SmartyPants Inc., Marina del Rey, CA 90292

Smartypants Vitamins

FDA Food Moderate Dec 12, 2018

Udderly Chocolate ice cream (item #67045), packaged in 1.75 qt. container. UPC 0 72830 07045 4. The label is read in parts: "***Tillamook*** ICE CREAM*** UDDERLY CHOCOLATE *** CONTAINS: MILK, TREE NUTS (COCONUT), SOY, EGG. IT IS MADE WITH EQUIPMENT THAT ALSO MAKES PRODUCTS CONTAINING PEANUTS, AND WHEAT.***"

TILLAMOOK COUNTY CREAMERY ASSOC

FDA Food Critical Dec 12, 2018

Tres Hermanos Bakery Telera and Bolillo Mexican White Bread, 1lb and 2 ounces per pkg

TRES HERMANOS BAKERY

FDA Food Moderate Dec 12, 2018

Vanilla Chocolate Chip ice cream (item #67017), packaged in 1.75 qt. container. UPC 0 72830 07017 1. The label is read in parts: "***Tillamook*** ICE CREAM*** VANILLA CHOCOLATE CHIP *** CONTAINS: MILK, TREE NUTS (COCONUT), EGG. IT IS MADE WITH EQUIPMENT THAT ALSO MAKES PRODUCTS CONTAINING PEANUTS, AND WHEAT.***"

TILLAMOOK COUNTY CREAMERY ASSOC

FDA Food Critical Dec 12, 2018

16 count Crunch & Pop Mix Variety Pack Sack

Frito-Lay, Inc.

FDA Food Moderate Dec 12, 2018

Sebastiano s Naturally Flavored Gourmet Syrups French Vanilla Naturally Sugar Free, Sweetened with Stevia; 25.4 fl. oz. (750 ml)

Frutarom USA Inc.

FDA Food Critical Dec 12, 2018

16 count Smartfood Delight Variety Pack Sack

Frito-Lay, Inc.

FDA Food Moderate Dec 12, 2018

Chocolate and Nut Tray. The product comes in a four-quadrant plastic tray, NET WT 37 OZ (2 LBS 5 OZ) 1.05KG, with UPC: 0 23637 43369 0.

First Source, LLC

FDA Food Moderate Dec 12, 2018

Italian Spice Blend Salt Free in 2 Lb. plastic bottles and 20 Lb. bulk boxes. Ingredients; Basil, Rosemary, Oregano, Marjoram & Spices. Not labeled for Resale.

Black River Industries

FDA Food Moderate Dec 12, 2018

Tickled PEACHES Freestone Dices; Net wt 4.4 oz. (125g) sealed plastic cups; KEEP FROZEN; Palmetto Processing Solutions 5 RW Dubose Road Ridge Spring, SC 29129 UPC 0110817134020432

Titan Farms, Inc. d/b/a Palmetto Processing Solutions

FDA Food Moderate Dec 12, 2018

Schnucks BIG & FLAKY CRESCENT ROLLS, 6 ROLLS, NET WT 11.25 OZ UPC 0 41318 57046 5

English Bay Batter L.P.

FDA Food Critical Dec 12, 2018

Ottogi Jin Ramen Spicy NET WT. 1lb 5.16oz, 600g (120gx5) 5PK Manufactured by: Ottogi Ramyon Co. Ltd. Distributed by: Ottogi America, Inc. 1650 W. El Segundo Bl. Gardena, CA 90249

Ottogi America Inc

FDA Food Critical Dec 12, 2018

Jay Robb Unflavored Egg White Protein, Net Weight 24 oz (1.5lbs) 680g. Dietary Supplement. UPC 03907-00492. Jay Robb, Inc., Jupiter, FL 33458

Agropur MSI Ingredients LLC

FDA Food Moderate Dec 12, 2018

Parsley Flakes in 6 oz. and 24 oz. plastic bottles and 20 lb boxes

Black River Industries

FDA Food Moderate Dec 12, 2018

Sweet Basil Leaf in 2 Lb. plastic bottles and 25 pound bulk boxes.

Black River Industries

FDA Food Critical Dec 12, 2018

Ottogi Jin Ramen Mild NET WT. 1lb 5.16oz, 600g (120gx5) 5PK Manufactured by: Ottogi Ramyon Co. Ltd. Distributed by: Ottogi America, Inc. 1650 W. El Segundo Bl. Gardena, CA 90249

Ottogi America Inc

FDA Food Moderate Dec 12, 2018

VANILLA WHIPPED ICING ARTIFICALLY FLAVORED Product Number: 09076 / UPC: 10049800090764

Rich Products Corp

FDA Drug Critical Dec 12, 2018

SODIUM CHLORIDE INJECTION, USP, 0.9%, 20 mL Single Dose Vial, packaged in a 25-unit tray, Rx Only, APP Pharmaceuticals, LLC Schaumburg, IL 60173. NDC 63323-186-20, Product code 918620

Fresenius Kabi USA, LLC

FDA Drug Critical Dec 12, 2018

SODIUM CHLORIDE INJECTION, USP, 0.9%, 10 mL Single Dose Vial, packaged in a 25-unit tray, Rx Only, APP Pharmaceuticals, LLC Schaumburg, IL 60173. NDC 63323-186-10 Product code 918610

Fresenius Kabi USA, LLC

FDA Drug Low Dec 12, 2018

Amlodipine and Olmesartan Medoxomil Tablets, 5 mg/40 mg, Rx only, 30-count bottle, Distributed by: Aurobindo Pharma USA, Inc. 279 Princeton-Hightstown Road East Windsor, NJ 0852 Made in India, NDC 65862-855-30

Aurobindo Pharma USA Inc.

FDA Devices Critical Dec 12, 2018

GE HEALTHCARE CARESCAPE R860 Inspiratory Safety Guard, Part Numbers: a) 2066713-001 (single pack) b) 2083208-001 (box of ten singles) The CARESCAPE R860 ventilator is designed to provide mechanical ventilation or support to neonatal, pediatric, and adult patients weighing 0.25 kg and above. The CARESCAPE R860 ventilator is a microprocessor based, electronically controlled, pneumatically driven ventilator that includes integrated monitoring of FiO2, airway pressure, flow, and volume.

GE Healthcare, LLC

FDA Devices Moderate Dec 12, 2018

Zimmer ZMS¿ Intramedullary Fixation Smooth Guide Wire, 2.4 mm Diameter, 100 cm Length Item Number: 47-2237-033-00 Product Usage: A single use surgical instrument used during orthopaedic surgery for implantation of a prosthesis.

Zimmer Biomet, Inc.

FDA Devices Low Dec 12, 2018

NEOCONNECT, Enteral Extension with ENFit connector, REF EXT-60NC The NeoMed NeoConnect Enteral Only Extension Set is intended for use as an extension set for nasogastric/oralgastric or gastric tube enteral feeding tubes, incorporating safety connectors which help mitigate the risk of accidental connection of an I.V. system to the enteral system or the enteral system to an I.V. system. This device is indicated for use in neonatal and pediatric patients in connection with an enteral feeding tu

Neomed Inc

FDA Devices Moderate Dec 12, 2018

Zimmer M/DN¿ Intramedullary Fixation Humeral Guide Wire - Bullet Tip, 2.4 mm Diameter, 70 cm Length Item Number: 00-2255-026-00 Product Usage: A single use surgical instrument used during orthopaedic surgery for implantation of a prosthesis.

Zimmer Biomet, Inc.

FDA Devices Moderate Dec 12, 2018

Biomet 20mm Compress Device Short Anchor Plug With Drill Set / With Pin Inserter Ion Implant Item number: 178562 Product Usage: 1. Correction of revision of unsuccessful osteotomy, arthrodesis, or previous joint replacement. 2. Tumor resections. 3. Revision of previously failed total joint arthroplasty. 4. Trauma. The Compress¿ Segmental Femoral Replacement System (Short Spindle and Anchor Plug) components are intended for uncemented use only.

Zimmer Biomet, Inc.

FDA Devices Moderate Dec 12, 2018

Zimmer Smooth Guide Wire - Bullet Tip, 3.0 mm Diameter, 100 cm Length Item Number: 47-2255-008-01 Product Usage: A single use surgical instrument used during orthopaedic surgery for implantation of a prosthesis.

Zimmer Biomet, Inc.

FDA Devices Moderate Dec 12, 2018

Zimmer ZMS¿ Intramedullary Fixation Smooth Guide Wire, 3.0 mm Diameter, 100 cm Length Item Number: 47-2237-037-00 Product Usage: A single use surgical instrument used during orthopaedic surgery for implantation of a prosthesis.

Zimmer Biomet, Inc.

FDA Devices Low Dec 12, 2018

Gel Alkaline Phosphatase Isoenzyme Control Kit: Gel Alkaline Phosphatase Isoenzyme Control Cat. No. 5104 1 x 2.0 mL FOR IN-VITRO DIAGNOSTIC USE Gel Alkaline Phosphatase Isoenzyme Control 20mL 001831 Alkaline Phosphatase Isoenzyme Control is to be used as a qualitative and/or quantitative control to aid in the identification of alkaline Phosphatase isoenzymes by electrophoresis.

Helena Laboratories, Inc.

FDA Devices Moderate Dec 12, 2018

Atrium 28Fr PVC Thoracic Catheter RIGHT ANGLE, Part No. 8128

Atrium Medical Corporation

FDA Devices Moderate Dec 12, 2018

Captus 700 Thyroid Uptake System, Model # 5430-3137 and 5430-3138

Capintec Inc

FDA Devices Moderate Dec 12, 2018

Invacare 9805 and 9805P Hydraulic Patient Lifts, Model Nos. 9805 and 9805P The intended use of a Non-AC-Powered patient lift is to lift and transfer a patient from one surface to another, as from a bed to a wheelchair. The device includes straps and a sling to support the patient.

Invacare Corporation

FDA Devices Moderate Dec 12, 2018

Brilliance 6 Slice (Air), Model 728256 Product Usage: Computed Tomography X-ray systems intended to produce cross-sectional Images of the body by computer reconstruction of X-ray transmission data taken at different angles and planes. These devices may include signal analysts and display equipment, patient and equipment supports, components, and accessories

Philips Medical Systems (Cleveland) Inc

FDA Devices Moderate Dec 12, 2018

Zimmer Natural Nail¿ System - Tear Drop Guide Wire, 2.4 mm Diameter, 100 cm Length Item Number: 47-2490-097-01 Product Usage: A single use surgical instrument used during orthopaedic surgery for implantation of a prosthesis.

Zimmer Biomet, Inc.

FDA Devices Moderate Dec 12, 2018

Thermacare HeatWraps Menstrual a) UPC 0573302002 b) UPC 0573302044 Product Usage: Provides heat therapy for temporary relief of minor menstrual cramp pain and associated back aches.

Pfizer Inc.

FDA Devices Moderate Dec 12, 2018

Brilliance 40, Model 728235 Product Usage: Computed Tomography X-ray systems intended to produce cross-sectional Images of the body by computer reconstruction of X-ray transmission data taken at different angles and planes. These devices may include signal analysts and display equipment, patient and equipment supports, components, and accessories

Philips Medical Systems (Cleveland) Inc

FDA Devices Moderate Dec 12, 2018

BD BBL Trypticase Soy Agar with 5% Sheep Blood, Catalog No. 221261, (non-selective, non-differential)

Becton Dickinson & Co.

FDA Devices Moderate Dec 12, 2018

Zimmer Natural Nail¿ System - Tear Drop Guide Wire, 2.4 mm Diameter, 70 cm Length Item Number: 47-2490-098-01 Product Usage: A single use surgical instrument used during orthopaedic surgery for implantation of a prosthesis.

Zimmer Biomet, Inc.

FDA Devices Moderate Dec 12, 2018

Brilliance 16 Slice (Power), Model 728240 Product Usage: Computed Tomography X-ray systems intended to produce cross-sectional Images of the body by computer reconstruction of X-ray transmission data taken at different angles and planes. These devices may include signal analysts and display equipment, patient and equipment supports, components, and accessories

Philips Medical Systems (Cleveland) Inc

FDA Devices Moderate Dec 12, 2018

Zimmer M/DN¿ Intramedullary Fixation Humeral Guide Wire - Smooth, 2.4 mm Diameter, 70 cm Length Item Number: 00-2255-025-00 Product Usage: A single use surgical instrument used during orthopaedic surgery for implantation of a prosthesis.

Zimmer Biomet, Inc.

FDA Devices Moderate Dec 12, 2018

Cascade Abrazo c-ACT-LR Test Card IVD FOR IN VITRO DIAGNOSTIC USE Store at 2 to 8 C HELENA LABORATORIES 003366 12/13(2) FOR EXPORT ONLY

Helena Laboratories, Inc.

FDA Devices Moderate Dec 12, 2018

Family Wellness First Aid Sterile Gauze Pad 3 in x 3 in, 10 CT. White, bleached, non-woven, rayon/polyester sterile Gauze Pad 3 inch x 3 inch, 12-ply 10 count cardboard box

ASO, LLC

FDA Devices Moderate Dec 12, 2018

Thermacare Muscle Pain Therapy HeatWraps: a) UPC 0573301314 b) UPC 0573301303 Product Usage: Provides heat therapy for temporary relief of minor muscular and joint aches and pains associated with overexertion, sprains, and arthritis.

Pfizer 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.