PlainRecalls

2017 Recalls

7,480 recalls · Page 97 of 150

2017 Recall Year Insight

Federal agencies issued 7,480 product recalls indexed by PlainRecalls in calendar year 2017. That represents about 8.91% of the 83,949 total recalls we track from 1995 through the present, and averages roughly 20.5 recalls per day across the FDA, CPSC, 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 150 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 0 critical, 47 moderate, and 3 lower-severity recalls. The page references 30 distinct recalling firms operating in 2 distinct product categories, with 50 of 50 records disclosing affected-unit counts. Issuing-agency distribution on this slice leans toward FDA Devices (47), 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, or NHTSA for the system-of-record on any specific recall. PlainRecalls indexes this archive for research and consumer awareness purposes.

FDA Drug Low Apr 26, 2017

Dye Free Allergy Softgel Gelatin Capsule, 15,000-count bulk drums, aenova/Swiss Caps USA, Inc., 14193 S.W. 119th Avenue, Miami, FL 33186, Product Co…

InnovaGel

FDA Drug Moderate Apr 26, 2017

Nystatin and Triamcinolone Acetonide Cream, USP, 100,000 USP nystatin units and 1 mg triamcinolone acetonide, distributed in a) 15 grams (NDC 51672-1…

Taro Pharmaceuticals U.S.A., Inc.

FDA Drug Low Apr 26, 2017

CLENZIderm M.D. Acne Treatment System, kit has 3 bottles a) Therapeutic Lotion (benzoyl peroxide 5% Acne Treatment) 47mL bottle, b) Daily Care Foamin…

Valeant Pharmaceuticals North America LLC

FDA Devices Moderate Apr 26, 2017

various polyethylene implants Sports Med Repicci II Tibial Components Product Usage: Partial knee replacement

Zimmer Biomet, Inc.

FDA Devices Moderate Apr 26, 2017

D-RAD, S.T. LOCKING SCREWS, T7, QTY: (1), STERILE R, in the following sizes: (a) 2.4MM X 10MM, RES 74692410 (b) 2.4MM X 12MM, RES 74692412 (c) 2.4…

Smith & Nephew, Inc.

FDA Devices Moderate Apr 26, 2017

Software version 4.44A utilized on the BD MAX System

BD LIFE SCIENCES

FDA Devices Moderate Apr 26, 2017

Access Ferritin Calibrators, Part No. 33025, Ref No. B50136C

Beckman Coulter Inc.

FDA Devices Moderate Apr 26, 2017

216 Wilson Frame Pads, Model # 5319-37; Used with Radiolucent Wilson Frames, model numbers 5319G and 5321G. General and Plastic Surgery: These …

Mizuho OSI

FDA Devices Moderate Apr 26, 2017

various polyethylene implants Knees Revision Tibial Tray Systems Oxford Partial Knee Orthopedic Salvage System Vanguard Complete Knee System V…

Zimmer Biomet, Inc.

FDA Devices Moderate Apr 26, 2017

BD Viper LT software, version 3.00H

Bd Diagnostic

FDA Devices Moderate Apr 26, 2017

Allura Xper Release 8.2 (Laird chiller is always installed); Allura Xper FD10 722026; Allura Xper FD10/10 722027; Allura Xper FD20/10 biplane 722029;…

Philips Electronics North America Corporation

FDA Devices Moderate Apr 26, 2017

Peri-Loc(R) VLP 3.5 MM X 6 MM SELF-TAPPING CORTEX SCREW, QTY: (1), STERILE R, REF 71801306 Orthopedic

Smith & Nephew, Inc.

FDA Devices Moderate Apr 26, 2017

Smith & Nephew ACUFEX TRUNAV Retrograde Drill 6.5MM Product Number: 72204039 The ACUFEX TRUNAV Retrograde Drill is intended for use in creating a b…

Smith & Nephew, Inc.

FDA Devices Moderate Apr 26, 2017

Proteus 235, Proton Therapy System

Ion Beam Applications S.A.

FDA Devices Moderate Apr 26, 2017

NEODENT CM Intraoral Scanbody, Article Number: 108.139

Instradent USA, Inc.

FDA Devices Low Apr 26, 2017

Arrow EZ-IO Needle Set 45 mm 15 ga, Ref 9079.

Teleflex Medical

FDA Devices Moderate Apr 26, 2017

INFINITY Internal Hex Healing Abutment, 4.5mm Platform, 4.7mm CW-3mm CH Straight; Product Code: 20145473 Product Usage: Non implantable dental …

Ace Surgical Supply Co., Inc.

FDA Devices Moderate Apr 26, 2017

Smith & Nephew ACUFEX TRUNAV Retrograde Drill 8.5MM Product Number: 72204043 The ACUFEX TRUNAV Retrograde Drill is intended for use in creating a …

Smith & Nephew, Inc.

FDA Devices Moderate Apr 26, 2017

Valleylab Laparoscopic Handset; Material # E2750; Laproscopic Handset Non-Sterile Bulk; Material # E2750NSB Product Usage: For use in 5mm cannu…

COVIDIEN MEDTRONIC

FDA Devices Moderate Apr 26, 2017

It is recommended for patients with weight/size between 4-22 lbs (1.8-10 kg). Part Number 0270-0429: GVL 2 Stat (box of 10 Stats). Part Number 05…

Verathon Inc

FDA Devices Moderate Apr 26, 2017

Smith & Nephew ACUFEX TRUNAV Retrograde Drill 7MM Product Number: 72204040 The ACUFEX TRUNAV Retrograde Drill is intended for use in creating a bac…

Smith & Nephew, Inc.

FDA Devices Moderate Apr 26, 2017

Ferno PROFlexx¿ Model 28Z Chair Cot

Ferno-Washington Inc

FDA Devices Moderate Apr 26, 2017

Artis zee, Angiographic x-ray system

Siemens Medical Solutions USA, Inc

FDA Devices Moderate Apr 26, 2017

various polyethylene implants BIO PLUG 10MM Product Usage: Non-weight bearing accessory. Sterile, optional speciality components that are n…

Zimmer Biomet, Inc.

FDA Devices Moderate Apr 26, 2017

The following systems are only affected if a Laird chiller is installed (11NC: 98960021599): Allura Xper Releases 3 to 8.1: Allura Xper FD10 (C+F). 7…

Philips Electronics North America Corporation

FDA Devices Moderate Apr 26, 2017

Smith & Nephew ACUFEX TRUNAV Retrograde Drill 11MM Product Number: 72204048 The ACUFEX TRUNAV Retrograde Drill is intended for use in creating a ba…

Smith & Nephew, Inc.

FDA Devices Moderate Apr 26, 2017

Smith & Nephew ACUFEX TRUNAV Retrograde Drill 12MM Product Number: 72204050 The ACUFEX TRUNAV Retrograde Drill is intended for use in creating a ba…

Smith & Nephew, Inc.

FDA Devices Moderate Apr 26, 2017

Smith & Nephew ACUFEX TRUNAV Retrograde Drill 7.5MM Product Number: 72204041 The ACUFEX TRUNAV Retrograde Drill is intended for use in creating a b…

Smith & Nephew, Inc.

FDA Devices Moderate Apr 26, 2017

D-RAD, 1.8MM X 16MM, LOCKING PEG, QTY: (1), STERILE R, RES 74671816 Orthopedic

Smith & Nephew, Inc.

FDA Devices Moderate Apr 26, 2017

various polyethylene implants Hips Active Articulation ArComXL Bearings Active Articulation E1 Bearings Arcos Taper Cap BIOLOX delta Option Hea…

Zimmer Biomet, Inc.

FDA Devices Moderate Apr 26, 2017

Smith & Nephew ACUFEX TRUNAV Retrograde Drill 8MM Product Number: 72204042 The ACUFEX TRUNAV Retrograde Drill is intended for use in creating a ba…

Smith & Nephew, Inc.

FDA Devices Moderate Apr 26, 2017

D-RAD, 2.4MMX 20MM, S.T. CORTEX SCREW, QTY: (1), STERILE R, RES 74682420 Orthopedic

Smith & Nephew, Inc.

FDA Devices Moderate Apr 26, 2017

Hemotherm CE, model 400CE, Heater-Cooling Device

Cincinnati Sub-Zero Products Inc

FDA Devices Moderate Apr 26, 2017

Laerdal Compact Suction Unit ¿ 4 under the following labels: 1) 300 ml (3.3 lbs) canister version - CATALOG #(s): 88006101 - LCSU 4, 300 ml Complete …

Laerdal Medical Corporation

FDA Devices Moderate Apr 26, 2017

Tapered SwissPlus Implant System, Model No. SPB10

Zimmer Dental Inc

FDA Devices Moderate Apr 26, 2017

Smith & Nephew ACUFEX TRUNAV Retrograde Drill 10MM Product Number: 72204046 The ACUFEX TRUNAV Retrograde Drill is intended for use in creating a ba…

Smith & Nephew, Inc.

FDA Devices Moderate Apr 26, 2017

various polyethylene implants Extremities, Shoulders and Elbows BioModular Shoulder System; Comprehensive Shoulder System; Comprehensive Reverse S…

Zimmer Biomet, Inc.

FDA Devices Moderate Apr 26, 2017

Soft Face "No Bounce" Mallet Model/Catalog: BIO-1-1090

Signal Medical Corporation

FDA Devices Moderate Apr 26, 2017

Alcon Patient Care Kits Product Usage: A Patient Care Kit is an assemblage of single-use medical devices and accessories designed by medical prof…

Alcon Research, Ltd.

FDA Devices Moderate Apr 26, 2017

Bush DL Ureteral Illuminating Catheter Set Bush SL Ureteral Illuminating Catheter Set

Cook Inc.

FDA Devices Moderate Apr 26, 2017

Vacutainer Tubes Vacutainer tubes are intended for clinical laboratory hematology studies including but not limited to lead level testing, FEP level…

Avid Medical, Inc.

FDA Devices Moderate Apr 26, 2017

UNIQ: UNIQ FD10 722026; UNIQ FD10/10 722027; UNIQ FD20/10 biplane 722029; UNIQ FD10 OR Table 722033; UNIQ FD10/10 OR Table 722034; UNIQ FD20/10 OR Ta…

Philips Electronics North America Corporation

FDA Devices Moderate Apr 26, 2017

Elcam Minimal Residual Volume Luer-activated Swabable-stockcock (MRVLS) 4w gxl:w1/r rbls Product Usage: indicated for fluid flow directional c…

Elcam Medical, Inc.

FDA Devices Moderate Apr 26, 2017

Merge Eye Station and Merge Eye Care PACS.

Merge Healthcare, Inc.

FDA Devices Moderate Apr 26, 2017

PGCL [poly (glycolide-co-caprolactone)] Absorbable Suture, Manufacturer CP Medical, Portland OR, Sterile, Product Codes L923, L459, L493, L762, L463,…

CP Medical Inc

FDA Devices Moderate Apr 26, 2017

various polyethylene implants Custom parts Product Usage: Custom

Zimmer Biomet, Inc.

FDA Devices Moderate Apr 26, 2017

Cordis S.M.A.R.T. Flex Vascular Stent System

Cordis Corporation

FDA Devices Moderate Apr 26, 2017

Smith & Nephew ACUFEX TRUNAV Retrograde Drill 9.5MM Product Number: 72204045 The ACUFEX TRUNAV Retrograde Drill is intended for use in creating a b…

Smith & Nephew, Inc.

FDA Devices Moderate Apr 26, 2017

SURESTEP Tray, Bardex I.C. Complete Care Drainage Bag, 2000 ml Drainage Bag, 16 Fr., Sterile.

C.R. Bard, Inc.

FDA Devices Moderate Apr 26, 2017

Smith & Nephew ACUFEX TRUNAV Retrograde Drill 9MM Product Number: 72204044 The ACUFEX TRUNAV Retrograde Drill is intended for use in creating a bac…

Smith & Nephew, Inc.

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: CPSC + NHTSA — consumer product and vehicle recall feeds for 2017