2017 Recalls
7,681 federal recalls indexed for 2017 · Page 149 of 154
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 19 critical, 31 moderate, and 0 lower-severity recalls. The page references 34 distinct recalling firms operating in 7 distinct product categories, with 33 of 50 records disclosing affected-unit counts. Issuing-agency distribution on this slice leans toward NHTSA (17), FDA Drug (13), FDA Devices (13), 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.
Methylcobalamin Injectable (Dr. Hall Kit) - 1,000 mcg/mL, 30 mL vial Kit, Compounded by Wells Pharmacy, Ocala, FL
Wells Pharmacy Network LLC
Trimix Injectable 30 mg/3 mg/60 mcg/mL, a) 2 mL, b) 5 mL and c) 10 mL vials, Compounded by Wells Pharmacy, Ocala, FL
Wells Pharmacy Network LLC
TriMix, Alprostadil/Phentolamine/Papaverine 30mcg/1mg/10mg/mL, (1 ML). Compounded by Tri-Coast Pharmacy
Tri-Coast Pharmacy
QUAD2 (PAP/PHEN/ALPROS/ATRO) 9 mg/1 mg/10 mg/0.1 mg/mL Injectable a) 2 mL and b) 5 mL vial, Compounded by Wells Pharmacy, Ocala, FL
Wells Pharmacy Network LLC
Dexpanthenol 250 mg/mL (30 ML). Compounded by Tri-Coast Pharmacy
Tri-Coast Pharmacy
Testosterone Enanthate in Grapeseed Oil Injectable, 200 mg/mL, 10 mL vial, Compounded by Wells Pharmacy, Ocala, FL
Wells Pharmacy Network LLC
Calm Me (Aminobutyric Acid (GABA) 50 mg/Magnesium Chloride 50 mg/Taurine 50 mg/Theanine (L) 50 mg/Tryptophan (L) 10 mg/Lidocaine HCL 10 mg/ml), (30 ML). Compounded by Tri-Coast Pharmacy.
Tri-Coast Pharmacy
L-Arginine HCL 100 mg/mL, (30 ML). Compounded by Tri-Coast Pharmacy
Tri-Coast Pharmacy
HCG 11,000 IU Vial. Compounded by Tri-Coast Pharmacy
Tri-Coast Pharmacy
HCG 5,000 IU Vial. Compounded by Tri-Coast Pharmacy.
Tri-Coast Pharmacy
Alprostadil 40 mcg/mL Injectable, 10 mL vials, Compounded by Wells Pharmacy Network LLC, Ocala FL
Wells Pharmacy Network LLC
Amino Acid Recover Eaze (50 ML), Phenylaline (L) 8 mg/ml + Tyrosine (L) 0.45 mg/ml + L-Taurine 0.7 mg/ml. Compounded by Tri-Coast Pharmacy.
Tri-Coast Pharmacy
Amino Energy Cocktail (30 ML), (Methionine (L) 12.5 mg/Inositol 25 mg/Choline Chloride 25 mg/Methylcobalamin 300 mcg/Carnitine (L) 125 mg/Thiamine HCL 50 mg/Riboflavin-5-Phosphate Sod 5 mg/Niacinamide 20 mg/Pyridoxine HCL 2 mg/Folic Acid 2 mg/Ascorbic Acid 50 mg/Chromium Picolinate 200 mcg/Glutamine (L) 30 mg/Lidocaine HCL 10 mg/mL). Compounded by Tri-Coast Pharmacy.
Tri-Coast Pharmacy
TVC Imaging System model TVC-MC9 , for the near-infrared examination of coronary arteries in patients undergoing invasive coronary angiography The TVC Imaging System is an intravascular imaging device that simultaneously assesses vessel composition and structure using near-infrared spectroscopy (NIRS) and intravascular ultrasound (IVUS). This dual-modality instrument performs near-infrared spectroscopic analysis of the vessel to detect lipid core-containing plaques of interest (LCP) displayed i
Infraredx, Inc.
Modular Necks: The Modular SMF(TM) and Modular REDAPT(TM) Hip Systems are indicated for individuals undergoing primary and revision surgery where other treatments or devices have failed in rehabilitating hips damaged as a result of trauma or non-inflammatory degenerative joint disease (NIDJD) or any of its composite diagnoses of osteoarthritis, avascular necrosis, traumatic arthritis, slipped capital epiphysis, fused hip, fracture of the pelvis, and diastrophic variant. Hip components are also
Smith & Nephew, Inc.
Modular REDAPT(TM) Hip Systems The Modular SMF(TM) and Modular REDAPT(TM) Hip Systems are indicated for individuals undergoing primary and revision surgery where other treatments or devices have failed in rehabilitating hips damaged as a result of trauma or non-inflammatory degenerative joint disease (NIDJD) or any of its composite diagnoses of osteoarthritis, avascular necrosis, traumatic arthritis, slipped capital epiphysis, fused hip, fracture of the pelvis, and diastrophic variant. Hip co
Smith & Nephew, Inc.
Boston Scientific, INGEVITY" MRI Leads, Sterile EO, RxOnly.
Boston Scientific Corporation
DR Systems Unity PACS software, now known as Merge Unity PACS software.
Merge Healthcare, Inc.
PreludeEASE Hydrophilic Sheath Introducer Dilator The Merit PreludeEASE Hydrophilic Sheath Introducer is intended to provide access and facilitate the percutaneous introduction of various devices into veins and/or arteries, including but not limited to the radial artery, while maintaining hemostasis for a variety of diagnostic and therapeutic procedures. The access needle with inner metal needle and outer plastic cannula is used to gain access to the vein or artery for placement of guide wires
Merit Medical Systems, Inc.
TRU-Balance 3 Power Positioning Systems, TB3 Lift/Tilt/Recline (Gen 1). Mobility Medical Device
Pride Mobility Products Corp
Modular SMF(TM) The Modular SMF(TM) and Modular REDAPT(TM) Hip Systems are indicated for individuals undergoing primary and revision surgery where other treatments or devices have failed in rehabilitating hips damaged as a result of trauma or non-inflammatory degenerative joint disease (NIDJD) or any of its composite diagnoses of osteoarthritis, avascular necrosis, traumatic arthritis, slipped capital epiphysis, fused hip, fracture of the pelvis, and diastrophic variant. Hip components are also
Smith & Nephew, Inc.
Gomco Circumcision Clamps with separate O-Ring Component: The device is packaged non-sterile and has no shelf-life The Gomco clamp is intended to be used for circumcision surgeries
Aesculap Implant Systems LLC
GalaSHAPE 3D; product code SH3D03, a medium size oval GalaSHAPE" 3D is indicated for use as a bioresorbable scaffold for soft tissue support and to repair, elevate and reinforce deficiencies where weakness or voids exist that require the addition of material to obtain the desired surgical outcome. This includes reinforcement of soft tissue in plastic and reconstructive surgery, and general soft tissue reconstruction. GalaSHAPE" 3D is also indicated for the repair of fascial defects that require
Tepha Incorporated
PROFEMUR(R) R RASP HANDLE, REF PPW38078, 1 EACH, NON-STERILE, MicroPort Orthopedics, Arlington, TN Instruments support the implantation of implants. Broach handles mate to the broach to allow for preparation of the femoral canal for the stem component to be implanted. This
MicroPort Orthopedics Inc.
Normal Saline Flush 0.9% USP Sodium Chloride Injection Syringe, 3 ml fill, 5 ml fill and 10 ml fill. Product codes: 1203, 1205, 1210, 1210-BP Product usage: Saline flush
Nurse Assist, Inc
G3 Opticage Expandable Interbody Fusion Device, Model No. 9180-00, 9180-01, 9180-06, 9180-07, 9180-17, 9101-00, 9101-06 The Opticage Expandable Interbody Fusion Device is a posterior lumbar intervertebral body fusion device and is indicated for use with autogenous bone graft in patients with degenerative disc disease (DDD) at one or two contiguous levels from L2-S1. These DDD patients may also have up to Grade I spondylolisthesis or retrolisthesis at the involved level(s). The Opticage Interbod
Interventional Spine Inc
Arctic Cat Recalls Snowmobiles Due to Fire Hazard (Recall Alert)
Arctic Cat Inc., of Thief River Falls, Minn.
Linon Home Décor Recalls Dressers Due to Tip-Over Hazard; Sold Exclusively at Wayfair.com (Recall Alert)
Linon Home Décor Products Inc., of Mineola, N.Y.
Textron Specialized Vehicles Recalls Bad Boy Off-Road Utility Vehicles Due to Risk of Serious Injury or Death; One Death and One Injury Reported
Textron Specialized Vehicles, Inc., of Augusta, Georgia
AUDI 2005-2009: AIR BAGS:FRONTAL:PASSENGER SIDE:INFLATOR MODULE
AUDI
SUBARU 2005-2009: AIR BAGS:FRONTAL:PASSENGER SIDE:INFLATOR MODULE
SUBARU
Active Kyds Recalls Children's Toy Shovels and Garden Tool Sets Due to Lead Violations; Sold Exclusively on Amazon.com (Recall Alert)
Active Kyds LLC, of Dassel, Minn.
Dunkin' Donuts Recalls Glass Tumblers Due to Laceration and Burn Hazards
Dunkin' Brands, Inc., of Canton, Mass.
Michaels Recalls Rock Salt Lamps Due to Shock and Fire Hazards
SporTex US, of New York
HONDA 2006-2012: AIR BAGS:FRONTAL:PASSENGER SIDE:INFLATOR MODULE
HONDA
ACURA,HONDA 2006-2012: AIR BAGS:FRONTAL:PASSENGER SIDE:INFLATOR MODULE
ACURA,HONDA
ACURA,HONDA 2005-2012: AIR BAGS:FRONTAL:PASSENGER SIDE:INFLATOR MODULE
ACURA,HONDA
INFINITI,NISSAN 2005-2012: AIR BAGS:FRONTAL:PASSENGER SIDE:INFLATOR MODULE
INFINITI,NISSAN
JAGUAR 2009-2012: AIR BAGS:FRONTAL:PASSENGER SIDE:INFLATOR MODULE
JAGUAR
FORD,LINCOLN,MERCURY 2005-2012: AIR BAGS:FRONTAL:PASSENGER SIDE:INFLATOR MODULE
FORD,LINCOLN,MERCURY
TESLA 2012: AIR BAGS:FRONTAL:PASSENGER SIDE:INFLATOR MODULE
TESLA
MITSUBISHI 2012: AIR BAGS:FRONTAL:PASSENGER SIDE:INFLATOR MODULE
MITSUBISHI
BMW 2007-2012: AIR BAGS:FRONTAL:PASSENGER SIDE:INFLATOR MODULE
BMW
MERCEDES-BENZ 2012: AIR BAGS:FRONTAL:PASSENGER SIDE:INFLATOR MODULE
MERCEDES-BENZ
SAAB,SUBARU 2005-2008: AIR BAGS:FRONTAL:PASSENGER SIDE:INFLATOR MODULE
SAAB,SUBARU
LAND ROVER 2007-2012: AIR BAGS:FRONTAL:PASSENGER SIDE:INFLATOR MODULE
LAND ROVER
SUBARU 2005-2012: AIR BAGS:FRONTAL:PASSENGER SIDE:INFLATOR MODULE
SUBARU
MAZDA 2007-2009: AIR BAGS:FRONTAL:PASSENGER SIDE:INFLATOR MODULE
MAZDA
Perfect Fit Meals, LLC Recalls Chicken Breast Product Due to Misbranding and Undeclared Allergens
LEXUS,PONTIAC,SCION,TOYOTA 2006-2012: AIR BAGS:FRONTAL:PASSENGER SIDE:INFLATOR MODULE
LEXUS,PONTIAC,SCION,TOYOTA
Nearby Recall Years
Browse recalls from adjacent calendar years to see how federal enforcement volume has shifted over time.
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.