PlainRecalls

2017 Recall Year Insight

Federal agencies issued 7,681 product recalls indexed by PlainRecalls in calendar year 2017. That represents about 7.36% of the 104,423 total recalls we track from 1995 through the present, and averages roughly 21.0 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 154 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 2017.

On this page of 50 records, severity classification shows 17 critical, 32 moderate, and 1 lower-severity recalls. The page references 26 distinct recalling firms operating in 6 distinct product categories, with 49 of 50 records disclosing affected-unit counts. Issuing-agency distribution on this slice leans toward FDA Devices (26), FDA Food (18), 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 2017 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 Nov 15, 2017

HEBVeggie Toss Kit Caulibit Mushroom Sauce, 11oz bags ; UPC -4122017706

Mann Packing Company, Inc.

FDA Food Critical Nov 15, 2017

Mann's Nourish Bowls Southwest Chipotle, 10.5 oz trays; UPC -716519036958- US; UPC - 716519036866 - Canada

Mann Packing Company, Inc.

FDA Food Moderate Nov 15, 2017

Market District Powerberry Mix covered in Dark Chocolate; Net Wt. 8 OZ.; Contains Soy; May Contain: Milk Manufactured in a plant that processes wheat, peanuts, tree nuts and eggs.; Distributed by Giant Eagle, Inc., Pittsburgh, PA 15238-2809

Giant Eagle, Inc.

FDA Food Critical Nov 15, 2017

Mann's Power Blend, 20 oz bags ; UPC -716519000416- US 10 oz. bags UPC -716519013119 - US and Canada

Mann Packing Company, Inc.

FDA Food Critical Nov 15, 2017

Premium Vegetable Tray, 2 lb. 14 oz.. UPC 24210800000 Sold in Albertson's and Safeway Stores packed in clear plastic trays and cups.

Albertsons Inc

FDA Food Critical Nov 15, 2017

Veggies w/ Dip, 8 oz. UPC 24201200000 Sold in Albertson's and Safeway Stores packed in clear plastic trays and cups.

Albertsons Inc

FDA Food Critical Nov 15, 2017

Rectangular Vegetable Tray, 72 OZ UPC 24222100000 Sold in Albertson's and Safeway Stores packed in clear plastic trays and cups.

Albertsons Inc

FDA Food Critical Nov 15, 2017

Mann's Family Favorites Brussels Sprouts, 12 oz bags; UPC 716519010354 - Canada; also sold under Archer Farms 12 oz bag; Manns 2 lb

Mann Packing Company, Inc.

FDA Food Critical Nov 15, 2017

Tomatoes Broccoli Cheese & Ranch Dip 530 cal. 8OZ UPC 24288700000 Sold in Albertson's and Safeway Stores packed in clear plastic trays and cups.

Albertsons Inc

FDA Food Critical Nov 15, 2017

Broccoli Slaw, 12 oz bags; Sold under the following brand names: Western Family UPC -062639352295 - Canada Archer Farms Brand - US: UPC 085239343142 HEB - US UPC - 4122097512 Little Salad Bar - US UPC -041498216047 Signature Farms - US UPC - 021130983391 16 oz. bag Walmart - US UPC 681131148207 Foodservice : Mann 4 x 3 lb. bags

Mann Packing Company, Inc.

FDA Food Critical Nov 15, 2017

Mann's Nourish Bowls Sesame Sriracha, 12 oz Tray; UPC -716519036811- US; UPC -716519036828 - Canada

Mann Packing Company, Inc.

FDA Food Critical Nov 15, 2017

Broccoli Carrots Cauliflower with Ranch Dip 330 cal, 9 oz.. UPC 24218800000 Sold in Albertson's and Safeway Stores packed in clear plastic trays and cups.

Albertsons Inc

FDA Food Critical Nov 15, 2017

Mann's Snacking Favorites Cheddar Pretzel Veggie Tray, 19.6 oz tray; UPC -716519020445 - US

Mann Packing Company, Inc.

FDA Food Critical Nov 15, 2017

Saut¿ Kit, 20 OZ UPC 24261300000 Sold in Albertson's and Safeway Stores packed in clear plastic trays and cups.

Albertsons Inc

FDA Food Critical Nov 15, 2017

Mann's Family Favorites Broccoli Carrots, 12 oz. bags UPC 716519013058 - US HEB brand - 12 oz. bag UPC 4122097508

Mann Packing Company, Inc.

FDA Food Moderate Nov 15, 2017

Market District Almonds covered in Dark Chocolate; Net Wt. 8 OZ.; Contains Soy; May Contain: Milk Manufactured in a plant that processes wheat, peanuts, tree nuts and eggs.; Distributed by Giant Eagle, Inc., Pittsburgh, PA 15238-2809

Giant Eagle, Inc.

FDA Food Critical Nov 15, 2017

Trader Joe's Kohlrabi Salad Blend, 10 OZ Bags UPC 0058 6146

Mann Packing Company, Inc.

FDA Food Critical Nov 15, 2017

Mann's Rainbow Salad, 12 oz bags; UPC -716519013089- US and Canada

Mann Packing Company, Inc.

FDA Drug Low Nov 15, 2017

Doan's Pain Relieving Cream with 4% Lidocaine Plus Menthol, (lidocaine 4%, menthol 1%), Net Wt. 2.75 oz. (77.3 g) Tube, Distributed by: Ducere Pharma, LLC New Hope, PA 18938 USA --- UPC 849648000023

Dr. Reddy's Laboratories, Inc.

FDA Drug Moderate Nov 15, 2017

Succinylcholine 20 MG/ML INJ (QUELICIN), 10 ML Vials, Rx only, Distributed by: ACE Surgical Co., Inc., Brockton, MA

Ace Surgical Supply Co., Inc.

FDA Drug Moderate Nov 15, 2017

Betadine Solution Swabstick Povidone-Iodine Solution USP, 10% Dist.by: Purdue Products LP. Stamford, CT 06901-3431 NDC 67618-153-01

Purdue Pharma, LP

FDA Devices Moderate Nov 15, 2017

Cobalt HV with Gentamicin, Cobalt Bone Cement 40GM, REF 402283, QTY 1, STERILE, Rx Only, Mfgr: BIOMET ORTHOPEDICS Cobalt MV and HV Bone Cement is indicated for use as bone cement in arthroplastic procedures of the hip, knee and other joints to fix plastic and metal prosthetic parts to living bone when reconstructions is necessary because of osteoarthritis, rheumatoid arthritis, traumatic arthritis, avascular necrosis, nonunion of fractures of the neck of the femur, sickle cell anemia osteoporos

Encore Medical, Lp

FDA Devices Moderate Nov 15, 2017

RX-2 COUDE Epidural Needle, 16g x 3.5in (8.9cm)TW, 10 units, Calibrated, Plastic Hub, Detachable Wing, Blunt Stylet, Sterile, Rx only, For Use with 19g or Smaller Catheter

Epimed International

FDA Devices Moderate Nov 15, 2017

Cobalt MV Bone Cement 40GM, REF 402438, QTY 1, STERILE, Rx Only, Mfgr: BIOMET ORTHOPEDICS Cobalt MV and HV Bone Cement is indicated for use as bone cement in arthroplastic procedures of the hip, knee and other joints to fix plastic and metal prosthetic parts to living bone when reconstructions is necessary because of osteoarthritis, rheumatoid arthritis, traumatic arthritis, avascular necrosis, nonunion of fractures of the neck of the femur, sickle cell anemia osteoporosis, secondary severe joi

Encore Medical, Lp

FDA Devices Moderate Nov 15, 2017

TUOHY Epidural Needle, 20g x 3.5in(8.9cm) TW, 10 units, Calibrated, Plastic Hub, Fixed Wing, Sterile, Rx only

Epimed International

FDA Devices Moderate Nov 15, 2017

WECK(R) from TELEFLEX Auto Endo5(R), Automatic Hem-o-lok(R) Clip Applier, REF AE05ML (IPN010797) Rx ONLY, STERILE EO

Teleflex Medical

FDA Devices Moderate Nov 15, 2017

RESONATE X4 CRT-D, Model G447, Sterile.

Boston Scientific Corporation

FDA Devices Moderate Nov 15, 2017

HARVEST TERUMOBCT, GCP-10 Graft Delivery Pack, REF 51449, Rx Only, STERILE EO Harvest Graph Delivery System is a disposable pack that takes the cell concentrate created while using the BMAC Procedure Packs and allows for hydration of bone graft material for application to the sites doctors deem necessary

Terumo BCT, Inc.

FDA Devices Moderate Nov 15, 2017

BD Vacutainer Sodium Polyanetholesulfonate 5.95 mg Sodium Chloride 14.4 mg Blood Collection Tubes for Microbiological Studies (8.3 mL * 16x100mm) Catalog No. 364960

Becton Dickinson & Company

FDA Devices Moderate Nov 15, 2017

RESONATE EL ICD VR, Model D432, Sterile.

Boston Scientific Corporation

FDA Devices Moderate Nov 15, 2017

Cobalt MV with Gentamicin, Cobalt Bone Cement 40GM, REF 402439, QTY 1, STERILE, Rx Only, Mfgr: BIOMET ORTHOPEDICS Cobalt MV and HV Bone Cement is indicated for use as bone cement in arthroplastic procedures of the hip, knee and other joints to fix plastic and metal prosthetic parts to living bone when reconstructions is necessary because of osteoarthritis, rheumatoid arthritis, traumatic arthritis, avascular necrosis, nonunion of fractures of the neck of the femur, sickle cell anemia osteoporos

Encore Medical, Lp

FDA Devices Moderate Nov 15, 2017

MOMENTUM X4 CRT-D, Model G138, Sterile.

Boston Scientific Corporation

FDA Devices Moderate Nov 15, 2017

Cobalt HV Bone Cement 40GM, REF 402282, QTY 1, STERILE, Rx Only, Mfgr: BIOMET ORTHOPEDICS Cobalt MV and HV Bone Cement is indicated for use as bone cement in arthroplastic procedures of the hip, knee and other joints to fix plastic and metal prosthetic parts to living bone when reconstructions is necessary because of osteoarthritis, rheumatoid arthritis, traumatic arthritis, avascular necrosis, nonunion of fractures of the neck of the femur, sickle cell anemia osteoporosis, secondary severe joi

Encore Medical, Lp

FDA Devices Moderate Nov 15, 2017

Delta Cup Beater  Positioner - Aligner, model # 9057.20.555 Used during implantation of the Delta Acetabular System

Limacorporate S.p.A

FDA Devices Moderate Nov 15, 2017

AERO IOL Injection System containing 10 Z28 Cartridges per box, Part #003500-0025-282, Sterile, Rx. The firm name on the label is Aaren Scientific Inc., Ontario, CA. Used to fold and insert the firm's IOL's.

Aaren Scientific Inc.

FDA Devices Moderate Nov 15, 2017

RESONATE EL ICD DR, Model D433, Sterile.

Boston Scientific Corporation

FDA Devices Moderate Nov 15, 2017

VIGILANT X4 CRT-D, Model G247, Sterile. Cardiac Resynchronization Therapy Defibrillators (CRT-Ds) are indicated for patients with heart failure who receive stable optimal pharmacologic therapy (OPT) for heart failure and who meet any one of the following classifications: (1) Moderate to severe heart failure (NYHA Class III-IV) with EF d 35% and QRS duration e 120 ms; (2) Left bundle branch block (LBBB) with QRS duration e 130 ms, EF d 30%, and mild (NYHA Class II) ischemic or nonischemic he

Boston Scientific Corporation

FDA Devices Moderate Nov 15, 2017

Custom surgical kits labeled as follows: (a) Suture Removal Set, 910-0002 (b) Instrument Set, INST03/20 (c) Suture Removal Set, SUT309/100 (d) Incision & Drainage Tray, INC03/20 (e) Suture Removal Set, SUT103/50 (f) General Purpose Tray, GPT010/25 (g) General Purpose Tray, GPT002/50

Bioseal Corporation

FDA Devices Moderate Nov 15, 2017

NucliSENS Lysis Buffer Extended lot for RES 76675

BioMerieux SA

FDA Devices Moderate Nov 15, 2017

AMS, ALIGNED MEDICAL SOLUTIONS, T&A Pack, AMS6357, STERILE EO.

Windstone Medical Packaging, Inc.

FDA Devices Moderate Nov 15, 2017

Custom Ti MAK RS OSS Segmental Femoral Rotating Hinged Knee. This Rotating Hinged Knee is intended to replace patient anatomy.

Zimmer Biomet, Inc.

FDA Devices Moderate Nov 15, 2017

Xper Flex Cardio PhysioMonitoring system The Xper Flex Cardio physiomonitoring system is used to facilitate invasive investigation of heart and vascular disease when non-invasive indicators warrant such. Its users, responsible to interpret the data made available, will be professional health care providers, such as physicians, registered nurses, cardiovascular technicians, radiology technicians, and other clinical health care providers. The Xper Flex Cardio physiomonitoring system may be used

Invivo Corporation

FDA Devices Moderate Nov 15, 2017

COUDE Blunt Nerve Block Needle, 10 units, 0.71mm (22 Ga) x 152mm, Each Unit Contains One Blunt Nerve Block Needle and One Wing, Sterile

Epimed International

FDA Devices Moderate Nov 15, 2017

VITEK2 GP-ID, REF 21342 IVD

Biomerieux Inc

FDA Devices Moderate Nov 15, 2017

North Star Imaging Inc. (NSI) Model X-7000 industrial cabinet x-ray system. Industrial x-ray imaging of product hardware

North Star Imaging Inc

FDA Devices Moderate Nov 15, 2017

FlexFlow Venous Cannula Model/Catalog Number 200-200 The FlexFlow Venous Cannula is a single use sterile device. It is a size 23 French with an outside diameter of 0.30 inch (7.7 mm) and an effective working length of 11.2 inch (28.5 cm). The FlexFlow Venous Cannula is an open lumen polymer tube incorporating wire reinforcement in distal sections. The distal sections of the cannula are perforated with multiple openings to allow increased fluid flow. The clear proximal section is not reinforced

Sorin Group USA, Inc.

FDA Devices Moderate Nov 15, 2017

Electrohydraulic lithotripter probe, 1.9 FR 375 cm, Model 9-195-371DS used with a Model 9-201-00 Autolith lithotripter. electrohydraulic lithotripsy (EHL) is a method that allows large stones to be fragmented and removed percutaneously or endoscopically.

Northgate Technologies, Inc.

CPSC No agency class Nov 15, 2017

Bush Hog Recalls Riding Lawn Mowers Due to Laceration Hazard

Bush Hog Inc., of Selma, Ala.

CPSC No agency class Nov 15, 2017

Wholesale Fireworks Recalls Fireworks Due to Violation of Federal Standards; Explosion and Burn Hazards

Wholesale Fireworks Inc., of Laramie, Wyo.

NHTSA No agency class Nov 15, 2017

BMW 2018: ELECTRICAL SYSTEM: INSTRUMENT CLUSTER/PANEL

BMW

Nearby Recall Years

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

Compare 2017 with 2016 →

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 2017

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 2017 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.