PlainRecalls

2017 Recalls

7,536 recalls · Page 117 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 0 critical, 50 moderate, and 0 lower-severity recalls. The page references 24 distinct recalling firms operating in 3 distinct product categories, with 50 of 50 records disclosing affected-unit counts. Issuing-agency distribution on this slice leans toward FDA Devices (42), FDA Drug (8), 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 Mar 22, 2017

MODIFIED JESSNER PEEL (Sal Acid 14%, Lactic Acid 14%, glycolic 14%), Rx only, Synergy RX, 4901 Morena Blvd # 504-A San Diego, CA 92117 (855) 792-6676

Synergy Rx

FDA Drug Moderate Mar 22, 2017

Triamcinolone 40 mg/mL 2 mL Single-Dose Vial for Injection, Preservative Free, Rx only, Compounded by Isomeric Pharmacy Solutions, Salt Lake City, U…

Isomeric Pharmacy Solution, LLC

FDA Drug Moderate Mar 22, 2017

SUPREME CREAM (Retinoic acid 0.05%, hydroquinone 6%, kojic acid 3%, Alpha Arbutin otc 2%, Azeliac acid 2%), Rx only, Synergy RX, 4901 Morena Blvd # 5…

Synergy Rx

FDA Drug Moderate Mar 22, 2017

RETINOIC ACID all strengths including 0.025%, 0.05% and 0.1% CREAM, RETINOIC ACID 0.025%/CLINDAMYCIN 1.2% GEL, RETINOIC ACID 0.025%/ HYALURONIC ACID…

Synergy Rx

FDA Drug Moderate Mar 22, 2017

BICARBONATE 10%, Rx only, Synergy RX, 4901 Morena Blvd # 504-A San Diego, CA 92117 (855) 792-6676

Synergy Rx

FDA Drug Moderate Mar 22, 2017

ADAPALENE 0.1%, BENZOYL PEROXIDE 2.5% GEL, ADAPELENE 0.3%, BENZOYL PEROXIDE 2,5% GEL, AZELAIC ACID 15% CREAM, AZELAIC ACID 20% IN OI FREE CREAM, Rx o…

Synergy Rx

FDA Drug Moderate Mar 22, 2017

RETINOIC ACID SOLUTION in all strengths including 0.3%, 0.4%, 0.5%, 1%, RETINOIC ACID SOLUTION LIQUID, 0.4%, Rx only, Synergy RX, 4901 Morena Blvd # …

Synergy Rx

FDA Drug Moderate Mar 22, 2017

TCA PEEL SOLUTION in all strengths including: 5%, 10%, 15%, 18%, and 20%, TCA 10%/LACTIC ACID 12%, TCA 6%/ LACTIC ACID12%, TCA 7%/SALICYLIC ACID 2% S…

Synergy Rx

FDA Devices Moderate Mar 22, 2017

Inion GRT Tack, drill bit and tack appl., 4x, Sterile. Is indicated for the surgical treatment of periodontal defects to aid in the regeneration …

Inion Ltd.

FDA Devices Moderate Mar 22, 2017

882480: BrightView designed for single or dual detector nuclear imaging accommodating a range of ECT studies. In addition it can be used to perform p…

Philips Medical Systems (Cleveland) Inc

FDA Devices Moderate Mar 22, 2017

L-Varlock Cage/Trial Implant Holder, Reference HD0060, Kisco International, France. Product Usage: The L-Varlock Lumbar Cage is indicated for int…

Kiscomedica S.A.

FDA Devices Moderate Mar 22, 2017

Bencox Mirabo PE Liner 36/44 Model Number: H1.L61.3644, UDI: 8806373852343

CORENTEC CO., LTD

FDA Devices Moderate Mar 22, 2017

Bivona¿ TTS (Tight to Shaft) Pediatric Tracheostomy Tube, Model No. 67SP035, Reorder No. 67SP035.

Smiths Medical ASD Inc.

FDA Devices Moderate Mar 22, 2017

ABL90 Flex Model #: 393-090 Portable, automated analyzer that measures pH, blood gases, electrolytes, glucose, lactate, bilirubin, and oximetry …

Radiometer America Inc

FDA Devices Moderate Mar 22, 2017

RTI Biologics BioSet IC RT Paste 2 cc Filler, bone void, calcium compound. Use in dental, spine and orthopedic applications

RTI Surgical, Inc.

FDA Devices Moderate Mar 22, 2017

LeMaitre Vascular Reddick Scoop Tip Cholangiogram Stiffer Catheter with Introducer (paper IFU) REF# 2401-53

LeMaitre Vascular, Inc.

FDA Devices Moderate Mar 22, 2017

Eclipse Hypodermic Needle

Becton Dickinson & Company

FDA Devices Moderate Mar 22, 2017

VASOVIEW HEMOPRO VH-3500 ENDOSCOPIC VESSEL HARVESTING SYSTEM Product Usage: The VASOVIEW HEMOPRO VH-3500 is designed for use in conjunction with…

Maquet Cardiovascular, LLC

FDA Devices Moderate Mar 22, 2017

Toshiba Kalare DREX-KL80 X-ray generator

Toshiba American Medical Systems Inc

FDA Devices Moderate Mar 22, 2017

Terumo Advanced Perfusion System 1-Level Sensor II Gel Pads Product Usage: Level sensor pads are used to attach the level sensors to a hard shell…

Terumo Cardiovascular Systems Corporation

FDA Devices Moderate Mar 22, 2017

LeMaitre Vascular Scoop Tip Cholangiogram Catheter with Introducer (paper IFU) REF# 2401-52

LeMaitre Vascular, Inc.

FDA Devices Moderate Mar 22, 2017

LeMaitre Vascular Reddick Cholangiogram Catheter with introducer(eIFU) REF # e2400-52

LeMaitre Vascular, Inc.

FDA Devices Moderate Mar 22, 2017

VITROS Chemistry Products Li (Lithium) Slides, REF/Catalog Number/Product Code 1632660 (18 slide format, 90 slides per sales unit) and REF/Catalog Nu…

Ortho-Clinical Diagnostics

FDA Devices Moderate Mar 22, 2017

Arkon Anesthesia Delivery System, Model 99999. Product Usage: Continuous Ventilator The Arkon Anesthesia Delivery System is designed to provide …

Del Mar Reynolds Medical, Ltd.

FDA Devices Moderate Mar 22, 2017

Artis Q and Q.Zen fluoroscopic x-ray system

Siemens Medical Solutions USA, Inc

FDA Devices Moderate Mar 22, 2017

LeMaitre Vascular Reddick Cholangiogram Stiffer Catheter with introducer (eIFU) REF # e2400-53

LeMaitre Vascular, Inc.

FDA Devices Moderate Mar 22, 2017

C2 CryoBalloon Ablation System - Controller Cap. C2 CryoBalloon Controller; Cryosurgical Unit, Cryogenic Surgical Device The affected product is th…

C2 Therapeutics, Inc.

FDA Devices Moderate Mar 22, 2017

LeMaitre Vascular Reddick Scoop Tip Cholangiogram Catheter (eIFU) REF# e2401-50

LeMaitre Vascular, Inc.

FDA Devices Moderate Mar 22, 2017

LeMaitre Vascular Scoop Tip Cholangiogram Catheter with Introducer (eIFU) REF# e2401-52

LeMaitre Vascular, Inc.

FDA Devices Moderate Mar 22, 2017

LeMaitre Vascular Reddick Scoop Tip Cholangiogram Catheter with Introducer (eIFU) REF# e2401-51

LeMaitre Vascular, Inc.

FDA Devices Moderate Mar 22, 2017

LeMaitre Vascular Reddick Scoop Tip Cholangiogram Stiffer Catheter (paper IFU) REF# 2401-50

LeMaitre Vascular, Inc.

FDA Devices Moderate Mar 22, 2017

LeMaitre Vascular Scoop Tip Cholangiogram Catheter with Introducer (eIFU) REF# e2401-53

LeMaitre Vascular, Inc.

FDA Devices Moderate Mar 22, 2017

BNX Fine Need Aspiration System (19GA); Material/Part #: DSN-19-01

Medtronic

FDA Devices Moderate Mar 22, 2017

SharkCore Fine Needle Biopsy System (22 GA); Material/Part #s: DSC-22-01

Medtronic

FDA Devices Moderate Mar 22, 2017

Artis Zee and Zeego fluoroscopic x-ray system

Siemens Medical Solutions USA, Inc

FDA Devices Moderate Mar 22, 2017

SharkCore Fine Needle Biopsy System (25GA); Material/Part#: DSC-25-01

Medtronic

FDA Devices Moderate Mar 22, 2017

882482: BrightView XCT 882454 BrightView X upgrade to XCT, designed for single or dual detector nuclear imaging accommodating a range of ECT studies.…

Philips Medical Systems (Cleveland) Inc

FDA Devices Moderate Mar 22, 2017

The ABL800 Model#:All

Radiometer America Inc

FDA Devices Moderate Mar 22, 2017

MaxGuard Extension Set with Injection Site and 0.2 micron filter, Model No. ME3305

CareFusion 303, Inc.

FDA Devices Moderate Mar 22, 2017

Terumo Advanced Perfusion System 1-Level Sensor II Pads, Product Usage: Ultrasonic couplant used to facilitate the transmission of sound energy …

Terumo Cardiovascular Systems Corporation

FDA Devices Moderate Mar 22, 2017

CADD Solis VIP Ambulatory Infusion Pump, Model 21-21210, Reorder 21-2120-0102-15,

Smiths Medical ASD, Inc.

FDA Devices Moderate Mar 22, 2017

SharkCore LG Fine Needle Biopsy System (19GA); Material/Part#: DSL-19-01

Medtronic

FDA Devices Moderate Mar 22, 2017

LeMaitre Vascular Reddick Cholangiogram Catheter (eIFU) REF# e2400-50

LeMaitre Vascular, Inc.

FDA Devices Moderate Mar 22, 2017

iConnect Enterprise Archive when used with RadSuite. The firm name on the label is Merge Healthcare.

Merge Healthcare, Inc.

FDA Devices Moderate Mar 22, 2017

.045 X 6 ST Guide Wire, Part number 45-0029-S, Sterile 10 pack of WS-1106ST and has a 6 inch length and 0.045 inch diameter. .054 X 7 ST Guide Wi…

Acumed LLC

FDA Devices Moderate Mar 22, 2017

MaxGuard Extension Set, Model No. ME2064, MP9009C, MP9209, MP9254C The MaxGuard extension sets are used to administer fluids from a container to a p…

CareFusion 303, Inc.

FDA Devices Moderate Mar 22, 2017

882478: BrightView X designed for single or dual detector nuclear imaging accommodating a range of ECT studies. In addition it can be used to perform…

Philips Medical Systems (Cleveland) Inc

FDA Devices Moderate Mar 22, 2017

OEC FlexiView 8800, Digital Mobile Imaging System, GE Medical Systems

GE OEC Medical Systems, Inc

FDA Devices Moderate Mar 22, 2017

LeMaitre Vascular Reddick Cholangiogram Stiffer Catheter with introducer (paper IFU) REF# 2401-51

LeMaitre Vascular, Inc.

FDA Devices Moderate Mar 22, 2017

LeMaitre Vascular Reddick Cholangiogram Stiffer Catheter (eIFU) REF# e2400-51

LeMaitre Vascular, 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

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 August 2026.