PlainRecalls

2017 Recalls

7,536 recalls · Page 44 of 151

2017 Recall Year Insight

Federal agencies issued 7,536 product recalls indexed by PlainRecalls in calendar year 2017. That represents about 7.41% of the 101,704 total recalls we track from 1995 through the present, and averages roughly 20.6 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 151 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 1 critical, 47 moderate, and 2 lower-severity recalls. The page references 26 distinct recalling firms operating in 5 distinct product categories, with 49 of 50 records disclosing affected-unit counts. Issuing-agency distribution on this slice leans toward FDA Devices (34), FDA Drug (12), CPSC (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 Moderate Aug 9, 2017

Divalproex Sodium Delayed Release Tablets, USP, 250 mg 100-count bottle (NDC 68382-032-01), b.) 500-count bottle (NDC 68382-032-05),Rx only, Manufact…

Zydus Pharmaceuticals USA Inc

FDA Drug Moderate Aug 9, 2017

Neut Sodium Bicarbonate 4% (2.4 mEq) Additive Solution 5 mL , a.) Single-dose vial (NDC 0409-6609-02), b.) 25 vial carton (NDC 0409-6609-25), Rx Only…

Hospira a Pfizer Company

FDA Drug Moderate Aug 9, 2017

Divalproex Sodium Delayed Release Tablets, USP, 125 mg, 100-count bottle Rx only, Manufactured by Cadila Healthcare Ltd, Ahmedabad, India, Distribut…

Zydus Pharmaceuticals USA Inc

FDA Drug Low Aug 9, 2017

Pravastatin Sodium Tablets, USP, 10 mg, packaged in a) 90-count bottles (NDC 55111-229-90) and b) 500-count bottles (NDC 55111-229-05), Rx only, Manu…

Dr. Reddy's Laboratories, Inc.

FDA Drug Moderate Aug 9, 2017

Carbamazepine Oral Suspension, USP. 100 mg/5 mL, 5 mL Unit Dose Cups, Rx Only, Pkg: Precision Dose, Inc., S. Beloit, IL 61080, NDC 68094-301-59.

Precision Dose Inc.

FDA Drug Moderate Aug 9, 2017

Testosterone Cypionate + Progesterone, 200 mg/ 2.5 mg/mL ,10 mL amber glass vials, Rx Only, Compounded by AXIA Pharmaceutical, Los Angeles, CA 90025

Fusion IV Pharmaceuticals, Inc. dba Axia Pharmaceutical

FDA Drug Moderate Aug 9, 2017

Divalproex Sodium Delayed Release Tablets, USP, 500 mg, a.) 100-count bottle (NDC 68382-033-01) b.) 500-count bottle (NDC 68382-033-05), Rx only, man…

Zydus Pharmaceuticals USA Inc

FDA Drug Moderate Aug 9, 2017

Famotidine Tablets USP, 20 mg, 100 count bottles, Rx only, Manufactured For: TEVA PHARMACEUTICALS USA, Sellersville, PA --- NDC 0172-5728-60

Teva Pharmaceuticals USA

FDA Drug Moderate Aug 9, 2017

Succinylcholine Chloride Injection, USP 200 mg (20 mg/mL) Quelicin Multiple-dose vial, 10 mL, For I.V. or I.M. use. a.) one vial (NDC: 0409-6629-02…

Hospira a Pfizer Company

FDA Drug Moderate Aug 9, 2017

Lactulose Solution, USP, 20 g/30 mL, dose cups delivers 30 mL packaged 50-unit dose cups per case, Manufactured by VistaPharm, Inc., Largo, FL 33771…

VistaPharm, Inc.

FDA Drug Low Aug 9, 2017

Albuterol Sulfate Inhalation Solution, 0.021% (0.63 mg/3mL), packaged in 5 pouches of 5 x 3mL Sterile Unit-Dose Vials For Inhalation per carton, Rx o…

Teva Pharmaceuticals USA

FDA Drug Moderate Aug 9, 2017

Cyclobenzaprine HCl Tablets, USP, 5 mg, 50 Tablets (5x10) Unit Dose Cartons, Rx Only, Manufactured for: AvKARE Inc, Pulaski, TN 38478 --- NDC: 50268-…

Apace KY LLC

FDA Devices Moderate Aug 9, 2017

SORIN GROUP, SMART PERFUSION PACK, SMART 1/4" PEDS PACK, REF 627262502, STERILE EO, Rx Only, 1 EA

Sorin Group USA, Inc.

FDA Devices Moderate Aug 9, 2017

Stroke Fast Pack(TM) Trevo XP ProVue Retriever 4 x 20, Trevo Pro 18 Microcatheter, AXS Catalyst 060x132CM - US, UPN M0033PK42022001

Stryker Neurovascular

FDA Devices Moderate Aug 9, 2017

SORIN GROUP, SMART PERFUSION PACK, SMART CIRCULATORY ASSIST PACK, REF 627255003, STERILE EO, Rx Only, 1 EA

Sorin Group USA, Inc.

FDA Devices Moderate Aug 9, 2017

Tomcat Instrument, REF ASY-07379, Hologic Incorporated, automated laboratory sample processing instrument.

Hologic, Inc

FDA Devices Moderate Aug 9, 2017

ROSA Brain, 3.0.0 The device is intended for the spatial positioning and orientation of instrument holders or tool guides to be used by neurosurgeon…

Zimmer Biomet, Inc.

FDA Devices Moderate Aug 9, 2017

ViaPeel PTFE Peelable Introducer 5FR, Part Number 10890-006

Greatbatch Medical

FDA Devices Moderate Aug 9, 2017

NON-STERILE SAMPLE, SORIN GROUP, SMART PERFUSION PACK, REF 627376401, 1 EA, NOT FOR CLINICAL USE

Sorin Group USA, Inc.

FDA Devices Moderate Aug 9, 2017

Oxford/Oxbridge AFN End Cap 10 mm x 5 mm tp 12 mm x10 mm The end caps are a circular disk with a small threaded shaft to be screwed to the dista…

Ortho Solutions Inc

FDA Devices Moderate Aug 9, 2017

Stroke Fast Pack(TM) Trevo XP ProVue Retriever 4 x 30, Trevo Pro 18 Microcatheter, AXS Catalyst 060x132CM - US, UPN M0033PK43022001

Stryker Neurovascular

FDA Devices Moderate Aug 9, 2017

Stroke Fast Pack(TM) Trevo XP ProVue Retriever 3 x 20, Trevo Pro 14 Microcatheter, AXS Catalyst 060x132CM - US, UPN M0033PK32021001

Stryker Neurovascular

FDA Devices Moderate Aug 9, 2017

SORIN GROUP, SMART PERFUSION PACK, INSPIRE 8FS S5 PACK W/CARDIOPLEGIA-3D, (a) REF 044042600 AND (b) REF 044011200, STERILE EO, Rx Only, 1 EA

Sorin Group USA, Inc.

FDA Devices Moderate Aug 9, 2017

Non-Locking screws in the following lengths: (a) NEO(R) 0.27 - 10 mm, REF W27 ST010 (b) NEO(R) 0.27 - 12 mm, REF W27 ST012 (c) DRP 0.27 - 12 mm, R…

In2Bones, SAS

FDA Devices Moderate Aug 9, 2017

InflammaDry(R) AN RPS DIAGNOSTIC SOLUTION, Sample Collectors InflammaDry(R) is a rapid, immunoassay test for the visual, qualitative, in vitro detec…

Quidel Corporation

FDA Devices Moderate Aug 9, 2017

SORIN GROUP, SMART PERFUSION PACK, INSPIRE 6FS, REF 044008204, STERILE EO, Rx Only, 1 EA

Sorin Group USA, Inc.

FDA Devices Moderate Aug 9, 2017

SORIN GROUP, SMART PERFUSION PACK, SMA PRIMO2X OPTI PACK, REF 088512900, STERILE EO, Rx Only, 1 EA

Sorin Group USA, Inc.

FDA Devices Moderate Aug 9, 2017

SORIN GROUP, SMART PERFUSION PACK, INSPIRE 8S, REF 044036101, STERILE EO, Rx Only, 1 EA

Sorin Group USA, Inc.

FDA Devices Moderate Aug 9, 2017

MULTIGENT Creatinine (Enzymatic), Catalog Numbers 8L24-31 and 8L24-41; IVD. Intended for the quantitative determination of creatinine in human serum…

Sentinel CH SPA

FDA Devices Moderate Aug 9, 2017

SORIN GROUP, SMART PERFUSION PACK, TOTAL VISION SYSTEM-SMA, REF 084510101, STERILE EO, Rx Only, 1 EA

Sorin Group USA, Inc.

FDA Devices Moderate Aug 9, 2017

Myelotec Video Guided Catheters, REF 2010 3.0 mm OD x 30 Cm Working Length, Two 1.3mm Working Channels

Myelotec, Inc.

FDA Devices Moderate Aug 9, 2017

GE Inspection Technologies Blade|line Industrial Cabinet X-ray system

GE Inspection Technologies, LP

FDA Devices Moderate Aug 9, 2017

SORIN GROUP, SMART PERFUSION PACK, PUMP AND TABLE PACK, REF 627374101, STERILE EO, Rx Only, 1 EA

Sorin Group USA, Inc.

FDA Devices Moderate Aug 9, 2017

Biosense Webster MobiCath Bi-Directional Guiding Sheath, Model D140010 (small curve) and D140011 (large curve). The MobiCath Bi-Directional Guidin…

Greatbatch Medical

FDA Devices Moderate Aug 9, 2017

NON-STERILE SAMPLE, SORIN GROUP, SMART PERFUSION PACK, INSPIRE 8FS, REF 044043700, 1 EA, NOT FOR CLINICAL USE

Sorin Group USA, Inc.

FDA Devices Moderate Aug 9, 2017

NON-STERILE SAMPLE, SORIN GROUP, SMART CARDIOPLEGIA, CARDIOPLEGIA PACK, REF 627366901, 1 EA, NOT FOR CLINICAL USE

Sorin Group USA, Inc.

FDA Devices Moderate Aug 9, 2017

SORIN GROUP, SMART PERFUSION PACK, LONG PACK, REF 088512600, STERILE EO, Rx Only, 1 EA

Sorin Group USA, Inc.

FDA Devices Moderate Aug 9, 2017

SORIN GROUP, SMART PERFUSION PACK, SMART 3/16" PEDS PACK, REF 627263601, STERILE EO, Rx Only, 1 EA

Sorin Group USA, Inc.

FDA Devices Moderate Aug 9, 2017

SoftLab Software Laboratory information system to be used in a medical research or clinical laboratory by knowledgeable, trained,

Soft Computer Consultants, Inc.

FDA Devices Moderate Aug 9, 2017

STERILE SAMPLE SORIN GROUP, SMART PERFUSION PACK, NEONATE/PEDIATRIC PACK, REF 627127703, STERILE EO, Rx Only, 1 EA

Sorin Group USA, Inc.

FDA Devices Moderate Aug 9, 2017

SORIN GROUP, SMART PERFUSION PACK, NEONATE/PEDIATRIC PACK, REF 627127702, STERILE EO, Rx Only, 1 EA

Sorin Group USA, Inc.

FDA Devices Moderate Aug 9, 2017

Olympus Scientific Solutions Americas Corporation (OSSA) Model: VANTA Analytical X-Ray System, X-Ray Fluorescence

Olympus Scientific Solutions Americas

FDA Devices Moderate Aug 9, 2017

Stroke Fast Pack(TM) Trevo XP ProVue Retriever 6 x 25, AXS Catalyst 060x132CM - US, EXCELSIOR XT 27 MICROCATHETER, UPN M0033PK62523001 ST 150

Stryker Neurovascular

FDA Devices Moderate Aug 9, 2017

OptiLITE(TM) Products for Laser Surgery, Catalog Numbers: HTM1020F, HTM1040F, HTM1060F, HTM1010F; Manufactured by CONVERGENT LASTER TECHNOLOGIES …

Xintec Corp

FDA Devices Moderate Aug 9, 2017

Spectranetics Turbo-Elite Laser Atherectomy Catheter Peripheral Rapid Exchange Catheters Device is indicated for use in the treatment, including at…

Spectranetics Corporation

FDA Devices Moderate Aug 9, 2017

SORIN GROUP, SMART PERFUSION PACK, SMART VENOUS VACUUM, REF 084118102, STERILE EO, Rx Only, 1 EA

Sorin Group USA, Inc.

CPSC Moderate Aug 8, 2017

Meijer Recalls Children's Swimsuits Due to Choking Hazard

Wholesale Merchandisers LLC, of Grand Rapids, Mich.

CPSC Moderate Aug 8, 2017

NVIDIA Recalls European Plug Heads Sold with Power Adaptors Due to Electric Shock Hazard

CPSC Moderate Aug 8, 2017

Polaris Recalls Scrambler All-Terrain Vehicles Due to Crash Hazard

Polaris Industries Inc., of Medina, Minn.

NHTSA Critical Aug 8, 2017

DODGE 2017: ENGINE AND ENGINE COOLING:ENGINE

DODGE

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

Every figure on PlainRecalls is rendered directly from official FDA, CPSC and NHTSA recall records, no number is typed in by an editor. Figures cover calendar year 2017 across the FDA, CPSC 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 July 2026.