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 6 critical, 41 moderate, and 3 lower-severity recalls. The page references 23 distinct recalling firms operating in 6 distinct product categories, with 46 of 50 records disclosing affected-unit counts. Issuing-agency distribution on this slice leans toward FDA Devices (26), FDA Food (12), FDA Drug (12), 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 Food Critical Mar 21, 2018

Testosterzone 180 count bottle packaged in an amber plastic bottle with a black cap

Progressive Laboratories, Inc

FDA Food Moderate Mar 21, 2018

Green Tea Clay; 2.1 and 0.17 oz. jars evanhealy Hand Made in CA by Plant Divas Inc., San Diego, CA 92064

Plant Devas Inc

FDA Food Critical Mar 21, 2018

Xenesta Nuvive Mens 90 count packaged in an white plastic bottle with white cap

Progressive Laboratories, Inc

FDA Food Moderate Mar 21, 2018

Lemongrass Facial Polish with Oats, Fengreek & Neem. 3 oz cylindrical box evanhealy Hand Made in CA by Plant Divas Inc., San Diego, CA 92064

Plant Devas Inc

FDA Food Critical Mar 21, 2018

Xenesta Nuvive Womens 90 count packaged in a white plastic bottle with white cap

Progressive Laboratories, Inc

FDA Food Moderate Mar 21, 2018

Maple Minis-Gluten Free, Donut Bites. Packaged in clam shell with label on top. 5 oz package. UPC 8 81314 32681 5. The product is read in parts: "***maple minis***5oz***Eatin' Alive***PLANT BASED NOSH***Keep Refrigerated***INGREDIENTS: GF OATS, COCONUT, MAPLE SYRUP, COCONUT OI, CHOCOLATE * (CACAO, RAW CANE SUGAR, COCOA BUTTER, VANILLA BEAN), VANILLA, SALT, CINNAMON. * ORGANIC***".

Paige Common

FDA Food Critical Mar 21, 2018

All-Natural Ciolo Nut-Free Basil Pesto, 7 oz., plastic container, Item #: 30019.18

Blue Moose of Boulder, LLC

FDA Food Moderate Mar 21, 2018

Rose Face Care Kit; Each kit contains: Rose Cleansing Milk -- 1 fl oz bottle Rose Geranium Facial Tonic HydroSoul 1 fl oz bottle Rosehip Treatment Facial Serum - ROSE 0.13 fl oz vial Rose Vetiver Day Moisturizer 0.17 fl oz jar French Rose Clay 0.1 oz jar evanhealy Hand Made in CA by Plant Divas Inc., San Diego, CA 92064

Plant Devas Inc

FDA Food Moderate Mar 21, 2018

Seviroli brand Cannoli Shells. Large Plain 36 ct., and Small Plain 72 ct.

Ariola Foods, Inc.

FDA Food Moderate Mar 21, 2018

Almond Love Bar - Vegan Chocolate Bar, wrapped in plastic wrap with label on top. 2.5 oz bar. UPC 0 91037 32678 2 The product is read in parts: "***almond love bar***2.5oz***Eatin' Alive***PLANT BASED NOSH***Keep Refrigerated***Ingredients: Crust (Almond, Coconut Oil, Cacao, Coconut Sugar, Salt), Almond Butter (Almonds, Maple Syrup, Salt), Chocolate *( Cacao, Raw Cane Sugar, Cacao Butter, Vanilla Bean) * Organic.***Keep Refrigerated***".

Paige Common

FDA Food Moderate Mar 21, 2018

Clay Mask Kit; 2 glass jars of clay: Green Tea Clay 0.3 oz., and French Rose Clay 0.4 oz. 1 fan mask brush; and 1 terra cotta mixing bowl. Ingredients: Green tea clay, Green (Montmorillonite) clay, Organic Green Tea (Camellia Sinensis) French Rose Clay, Rose Clay (Kaolin Clay) Rhassonl Clay (Moroccan Lava Clay. evanhealy Hand Made in CA by Plant Divas Inc., San Diego, CA 92064

Plant Devas Inc

FDA Food Moderate Mar 21, 2018

Blue Face Care Kit; Each kit contains: Blue Lavender Cleansing Milk 1 fl oz bottle Lavender Facial Tonic HydroSoul 1 fl oz bottle Rosehip Treatment Facial Serum - BLUE 0.13 fl oz vial Blue Chamomile Day Moisturizer 0.17 fl oz jar Green Tea Clay 0.1 oz jar evanhealy Hand Made in CA by Plant Divas Inc., San Diego, CA 92064

Plant Devas Inc

FDA Drug Low Mar 21, 2018

Clocortolone Pivalate Cream, 0.1%, 90-gram tube, Rx only, Distributed by: Dr. Reddy's Laboratories, Inc. Princeton, NJ 08540, Manufactured by: DPT, Laboratories Ltd. San Antonio, TX 78215, NDC 43598-341-90

Dr. Reddy's Laboratories, Inc.

FDA Drug Low Mar 21, 2018

Lupin Hydrocodone Bitartrate and Homatropine Methylbromide Tablets, USP 5/1.5 mg Rx Only 30 Tablets Manufactured by: Novel Laboratories, Inc. Somerset, NJ 08873 Manufactured for: Lupin Pharmaceuticals, Inc. Baltimore, MD 21202 NDC 43386-118-03 UPC 343386118038

Novel Laboratories, Inc.

FDA Drug Low Mar 21, 2018

Psoriasin Daytime Relief Cream with Vitamin D & Oatmeal, (Coal Tar 1.25%), packagedin 57 g plastic tubes, Distributed by: ALVA-AMCO Pharmacal Cos., Inc., Niles, IL 60714, USA. NDC 52389-745-56, UPC 0 72959 01045 4.

Alva-Amco Pharmacal Companies., Inc.

FDA Drug Critical Mar 21, 2018

Hydromorphone, Hydrochloride, Injection, USP CII, 10 mg/mL, Rx Only, 1 mL Single-dose Vial, High Potency Formulation. Hospira, Inc., Lake forest, IL 60045 USA. NDC: 0409-2634-01

Pfizer Inc.

FDA Drug Moderate Mar 21, 2018

Valacyclovir Tablets USP 1 gram, 30-count bottle, Rx Only, Manufactured for Camber Pharmaceuticals, Inc. Piscataway, NJ 08854 By: Hetero Hetero Labs Limit Unit V Pollypally Jadcherla Mahaboob Nagar - 509 301 India NDC # 31722-705-30

Hetero Labs Limited Unit V

FDA Drug Moderate Mar 21, 2018

methylPREDNISolone Sodium Succinate for Injection, USP, 40 mg* per vial, Single-Dose Vial, Rx only, Mfd. for: Sagent Pharmaceuticals, Schaumburg, IL 60195 (USA), Made in India. NDC 25021-807-05.

Sagent Pharmaceuticals Inc

FDA Drug Moderate Mar 21, 2018

Valganciclovir Tablets, USP, 450 mg, 60-count bottle, Rx Only, Manufactured for Camber Pharmaceuticals, Inc. Piscataway, NJ 08854, By: Hetero Hetero Labs Limit Unit V Pollypally Jadcherla Mahaboob Nagar - 509 301 India. NDC # 31722-832-60

Hetero Labs Limited Unit V

FDA Drug Moderate Mar 21, 2018

methylPREDNISolone Sodium Succinate for Injection, USP, 1 gram* per vial, Single-Dose Vial, Rx only, Mfd. for: Sagent Pharmaceuticals, Schaumburg, IL 60195 (USA), Made in India. NDC 25021-810-30.

Sagent Pharmaceuticals Inc

FDA Drug Moderate Mar 21, 2018

Oxytocin USP, powder, 1g-bottle, API American Pharmaceutical Ingredients, NDC 58597-7042-3

American Pharmaceutical Ingredients LLC

FDA Drug Moderate Mar 21, 2018

methylPREDNISolone Sodium Succinate for Injection, USP, 125 mg* per vial, Single-Dose Vial, Rx only, Mfd. for: Sagent Pharmaceuticals, Schaumburg, IL 60195 (USA), Made in India. NDC 25021-808-10.

Sagent Pharmaceuticals Inc

FDA Drug Critical Mar 21, 2018

Hydromorphone, Hydrochloride, Injection, USP CII, 10 mg/mL, Rx Only, 1 mL Single-dose Vial, High Potency Formulation. Mfd For: Teva Parenteral Medicines, Inc., Irvine, CA 92618. NDC: 0703-0110-01

Pfizer Inc.

FDA Drug Moderate Mar 21, 2018

Sermorelin Acetate, powder, a) 1 GM-bottle (NDC58597-8092-1) b) 5 GM-bottle (NDC 58597-8092-2) c) 10 GM-bottle (NDC 58597-8092-4) API American Pharmaceutical Ingredients

American Pharmaceutical Ingredients LLC

FDA Devices Moderate Mar 21, 2018

PORT-A-CATH II PS/Titan, Tray PAC II. Labeled as: a. VEN LP, PU, 2.6MM, UL, 8.5FR/INTRO (1/EA); b. DL, LP, PU, 2.2MM, WING-LOCK, 7FR/INTRO (1/EA); c. DL, LP, PU, 3.2MM, WING-LOCK, 10FR/INTRO (1/EA)

Smiths Medical ASD Inc.

FDA Devices Moderate Mar 21, 2018

NovaKone Toric Daily Wear Soft contact; Catalog Number: AONKT54 Product Usage: The NOVAKONE TORIC lens is indicated for daily wear for persons requiring keratoconus management for the correction of refractive ametropia (myopia, hyperopia and astigmatism) in aphakic and not aphakic persons with otherwise non-diseased eyes and who possess refractive astigmatism not exceeding 10 Diopters.

Alden Optical

FDA Devices Moderate Mar 21, 2018

CPT 12/14 COCR SIZE 0 STD prosthesis, hip, semi-constrained, metal/polymer, porous uncemented

Zimmer Biomet, Inc.

FDA Devices Moderate Mar 21, 2018

VERSYS 6 INCH BEADED FC 13X160MM LM BODY EXT NECK & STD NECK Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented

Zimmer Biomet, Inc.

FDA Devices Moderate Mar 21, 2018

LPS PRECOAT FEM SIZE D-RT LPS PRECOAT FEM SIZE E-RT LPS POROUS FEM SIZE F-RT This device is indicated for patients with severe knee pain and disability

Zimmer Biomet, Inc.

FDA Devices Moderate Mar 21, 2018

Coons Interventional Wire Guide

Cook Inc.

FDA Devices Moderate Mar 21, 2018

Movable Core Wire Guide

Cook Inc.

FDA Devices Moderate Mar 21, 2018

STA - Neoplastine¿ Cl Plus ¿ (ref. 00606) Product Usage: Manual or automated determination of the prothrombin time (PT).

Diagnostica Stago, Inc.

FDA Devices Moderate Mar 21, 2018

BD Vacutainer¿ K2 EDTA (K2E) 3.6mg Blood Collection Tube (13 x 75 mm x 2.0 mL). Catalog Number: 367841. Used for whole blood hematology determinations, immunohematology testing and blood donor screening.

Becton Dickinson & Company

FDA Devices Moderate Mar 21, 2018

MAHURKAR"* Elite 12 FR x 16cm Acute Dual Lumen Dialysis Catheter with Curved Extensions, IC Trays. Product Number: 8888222316.

Medtronic Minimally Invasive Therapies Group

FDA Devices Moderate Mar 21, 2018

ARROWg+ard BLUE PLUS Pressure Injectable Two- 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 incompati

Arrow International Inc

FDA Devices Moderate Mar 21, 2018

Neoplastine¿ Cl Plus ¿ (ref. 00375) Product Usage: Manual or automated determination of the prothrombin time (PT).

Diagnostica Stago, Inc.

FDA Devices Moderate Mar 21, 2018

CR OPTION FEM COMP SIZE C/L CR OPTION FEM COMP SIZE C/R CR OPTION FEM COMP SIZE D/L CR OPTION FEM COMP SIZE D/R CR OPTION FEM COMP SIZE E/L CR OPTION FEM COMP SIZE E/R CR OPTION FEM COMP SIZE F/L CR OPTION FEM COMP SIZE F/R CR OPTION FEM COMP SIZE G/L CR OPTION FEM COMP SIZE G/R This device is indicated for patients with severe knee pain and disability

Zimmer Biomet, Inc.

FDA Devices Moderate Mar 21, 2018

Amplatz Extra Stiff Wire Guide

Cook Inc.

FDA Devices Moderate Mar 21, 2018

STA - Neoplastine¿ Cl ¿ (ref. 00605) Product Usage: Manual or automated determination of the prothrombin time (PT).

Diagnostica Stago, Inc.

FDA Devices Moderate Mar 21, 2018

ACE (TM) BRAND, DELUXE ANKLE BRACE, 207736, UPC 0 51131 20387 7

3M Company - Health Care Business

FDA Devices Moderate Mar 21, 2018

Amplatz Ultra Stiff Wire Guide

Cook Inc.

FDA Devices Moderate Mar 21, 2018

LPS-FLEX OPTION FEMORAL C-L LPS-FLEX OPTION FEMORAL C-L LPS-FLEX OPTION FEMORAL C-R LPS-FLEX OPTION FEMORAL D-L LPS-FLEX OPTION FEMORAL D-R LPS-FLEX OPTION FEMORAL E-L LPS-FLEX OPTION FEMORAL E-R LPS-FLEX OPTION FEMORAL F-L LPS-FLEX OPTION FEMORAL F-R LPS-FLEX OPTION FEMORAL G-L LPS-FLEX OPTION FEMORAL G-R This device is indicated for patients with severe knee pain and disability

Zimmer Biomet, Inc.

FDA Devices Moderate Mar 21, 2018

Bentson Cerebral Wire Guide

Cook Inc.

FDA Devices Moderate Mar 21, 2018

ARROWg+ard Blue¿ MAC" Two-Lumen Central Venous Access 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 m

Arrow International Inc

FDA Devices Moderate Mar 21, 2018

Vygon IV Start Convenience Kits; Product Codes AMS-623T and AMS-626TGSLF. Kit used when administering IV during emergency.

Vygon MFG, Inc., dba/ Churchill Medical Systems, Inc.

FDA Devices Moderate Mar 21, 2018

Femoral Artery Pressure Monitoring Set

Cook Inc.

FDA Devices Moderate Mar 21, 2018

Reuter Tip Deflecting Wire Guide

Cook Inc.

FDA Devices Moderate Mar 21, 2018

Pressure Injectable Multi- Lumen Central Venous Pressure Injectable ARROW(R) PICC Kit with Chlorag+ard(R) Technology 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

Arrow International Inc

FDA Devices Moderate Mar 21, 2018

Neoplastine¿ Cl Plus @ (ref.00374) Product Usage: Manual or automated determination of the prothrombin time (PT).

Diagnostica Stago, Inc.

FDA Devices Moderate Mar 21, 2018

OneStep CPR Complete, Adult Multi Function Electrodes, Part Numbers: 8900 0214 01 (case of 8 single electrodes, UDI: 10847946016279) and 8900 0224 01 (single electrode, UDI: 00847946016272) Product Usage: Intended Use: Defibrillation, Cardioversion, Noninvasive Pacing, EGG Monitoring, CPR Sensor. For use with ZOLL¿ Defibrillators: R Series, M Series. By Trained Personnel only, Including: Physicians, Nurses, Paramedics, Emergency Medical Technicians, Cardiovascular Laboratory Technicians.

ZOLL Medical Corporation

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.