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 14 critical, 36 moderate, and 0 lower-severity recalls. The page references 30 distinct recalling firms operating in 6 distinct product categories, with 42 of 50 records disclosing affected-unit counts. Issuing-agency distribution on this slice leans toward FDA Devices (18), FDA Food (16), NHTSA (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, USDA FSIS, or NHTSA for the system-of-record on any specific recall. PlainRecalls indexes this archive for research and consumer awareness purposes.

FDA Devices Moderate Jul 19, 2017

Nicolet¿ Elite¿ 2 MHz OB Probe, Non-Fetal Monitor, Model #: X1L007, Catalog Code: N200. Intended for non-invasive support, i.e. early detection of fetal life, monitor blood flow before and after surgery, etc.

Natus Neurology Inc

FDA Devices Moderate Jul 19, 2017

28 cm (11") PUR Smallbore Ext Set w/6-Port NanoClave¿ Manifold, Check Valve, NanoClave¿, Rotating Luer. Product Usage: The device is a single use, sterile, non-pyrogenic device which provides access for the administration of fluids from a container to a patients vascular system through the administration sets needle or catheter (which is inserted into a vein).

ICU Medical, Inc.

FDA Devices Moderate Jul 19, 2017

The Plum A+ Infusion Systems are a multipurpose family of devices that provides precise delivery of multiple therapies across the general spectrum of clinical care. The Plum A+ family infusion pumps are self contained, microprocessor based infusion devices. The pumps are available in single channel and in triple channel pumping mechanism types.

ICU

FDA Devices Moderate Jul 19, 2017

18 cm (7") PUR Smallbore Ext Set w/6-Port NanoClave¿ Manifold, Check Valve, NanoClave¿, Rotating Luer. Product Usage: The device is a single use, sterile, non-pyrogenic device which provides access for the administration of fluids from a container to a patients vascular system through the administration sets needle or catheter (which is inserted into a vein).

ICU Medical, Inc.

FDA Devices Moderate Jul 19, 2017

Burn Relief¿, MODEL #(s): 06BK1221, 06BK1232, 06BK1201, 06BK1200, CATALOG #(s): 06BK1221, 06BK1232, 06BK1201, 06BK1200 --- DRESSING,WOUND,HYDROGEL W/OUT DRUG AND/OR BIOLOGIC. --- Burn Relief¿ products are self-cooling, non-adhering and are intended to be used on 1st and 2nd degree burns.

O-Two Medical Technologies, Inc.

FDA Devices Moderate Jul 19, 2017

XARIO 100 TUS-X100 diagnostic ultrasound system

Toshiba American Medical Systems Inc

FDA Devices Moderate Jul 19, 2017

10" Smallbore Ext Set w/6-Port NanoClave¿ Manifold (Orange, Red, Blue, Purple, Yellow Rings), Check Valve, Clamp, Rotating Luer. Product Usage: The device is a single use, sterile, non-pyrogenic device which provides access for the administration of fluids from a container to a patients vascular system through the administration sets needle or catheter (which is inserted into a vein).

ICU Medical, Inc.

FDA Devices Moderate Jul 19, 2017

PROXIMALE - 28 cm (11") Smallbore Ext Set w/6-Port NanoClave¿ Manifold, Check Valve, NanoClave¿ (Red Rings), Rotating Luer. Product Usage: The device is a single use, sterile, non-pyrogenic device which provides access for the administration of fluids from a container to a patients vascular system through the administration sets needle or catheter (which is inserted into a vein)..

ICU Medical, Inc.

FDA Devices Moderate Jul 19, 2017

ArjoHuntleigh Flowtron ACS900, medical pump, software V1.099 Device is used to prevent the occurrence of Deep Vein Thrombosis (DVT) in at-risk patients. The system must be used as part of a prescribed plan of car under the supervision of trained medical and/or Clinical staff. The system is intended for use only in professional healthcare facilities. It is not intended to be used in the home healthcare environment.

Arjo, Inc. dba ArjoHuntleigh

FDA Devices Moderate Jul 19, 2017

APLIO i-series: a) APLIO i700 TUS AI700 b) APLIO i800 TUS AI800 diagnostic ultrasound system

Toshiba American Medical Systems Inc

FDA Devices Moderate Jul 19, 2017

Nicolet¿ Elite¿ 5 MHz Vascular Probe, Model #: X1L004, Catalog Code: N500. Intended for non-invasive support, i.e. early detection of fetal life, monitor blood flow before and after surgery, etc.

Natus Neurology Inc

FDA Devices Moderate Jul 19, 2017

Kit w/3 Ext Sets, 3 Drop-In MicroClave¿ Clear. Product Usage: The device is a single use, sterile, non-pyrogenic device which provides access for the administration of fluids from a container to a patients vascular system through the administration sets needle or catheter (which is inserted into a vein).

ICU Medical, Inc.

FDA Devices Moderate Jul 19, 2017

APLIO 300 TUS-A300 diagnostic ultrasound system

Toshiba American Medical Systems Inc

FDA Devices Moderate Jul 19, 2017

The Plum A+ Infusion Systems are a multipurpose family of devices that provides precise delivery of multiple therapies across the general spectrum of clinical care. The Plum A+ family infusion pumps are self contained, microprocessor based infusion devices. The pumps are available in single channel and in triple channel pumping mechanism types.

ICU

FDA Devices Moderate Jul 19, 2017

The Plum A+ Infusion Systems are a multipurpose family of devices that provides precise delivery of multiple therapies across the general spectrum of clinical care. The Plum A+ family infusion pumps are self contained, microprocessor based infusion devices. The pumps are available in single channel and in triple channel pumping mechanism types.

ICU

FDA Devices Critical Jul 19, 2017

ATAR Reusable Extension Cable, sold under brand names: ATAR Reusable Series, ATAR 53912 Reusable Series, and XI Reusable Series. Model codes: 53912 - MDTS ATAR REUSABLE, 53912A - MDTS ATAR REUSABLE, ATAR MDTS REUSABLE, ATAR-A DARK BLUE REUSABLE, ATAR-MDT REUSABLE, ATAR-MDT2 REUSABLE, ATAR-MDT2S-A, DK BLUE 30CM REUSABLE, ATAR-MDT2S-V WHITE 30CM REUSABLE, ATAR-MDTL REUSABLE, ATAR-MDTR REUSABLE, ATAR-R REUSABLE, ATAR-R T4P REUSABLE, ATAR-R1 REUSABLE, ATAR-RL REUSABLE, ATAR-T REUSABLE, ATAR-V W

Oscor, Inc.

FDA Devices Moderate Jul 19, 2017

Nicolet¿ Elite¿ 2 MHz OB Water Proof Probe, Model #: X1L008, Catalog Code: NW20. Intended for non-invasive support, i.e. early detection of fetal life, monitor blood flow before and after surgery, etc.

Natus Neurology Inc

FDA Devices Moderate Jul 19, 2017

Nova Biomedical Stat Profile Prime Analyzer as follows: PN 52855 Stat Profile Prime ABG Analyzer PN 53655 Stat Profile Prime ABG Analyzer with Scanner PN 52856 Stat Profile Prime CCS Analyzer PN 53656 Stat Profile Prime CCS Analyzer with Scanner PN 53657 Stat Profile Prime CCS Comp Analyzer with Scanner PN 52857 Stat Profile Prime CCS Comp Analyzer Blood Gas/Electrolyte/Metabolite/CO-Oximetry Analyzer

Nova Biomedical Corporation

CPSC No agency class Jul 19, 2017

Polaris Recalls Sportsman 570 All-Terrain Vehicles Due to Fuel Leak, Fire Hazards

Polaris Industries Inc., of Medina, Minn.

NHTSA No agency class Jul 19, 2017

FREIGHTLINER 2018: FUEL SYSTEM, DIESEL

FREIGHTLINER

CPSC No agency class Jul 18, 2017

Corbeau USA Recalls Camlock Seat Harness Belts Due to Fall and Projectile Hazards

Corbeau USA, LLC., of Bluffdale, Utah

CPSC No agency class Jul 18, 2017

Polaris Recalls RZR 570 and RZR S 570 Recreational Off-Highway Vehicles Due to Crash and Injury Hazards (Recall Alert)

Polaris Industries Inc., of Medina, Minn.

NHTSA No agency class Jul 18, 2017

MAZDA 2007-2012: AIR BAGS:FRONTAL:PASSENGER SIDE:INFLATOR MODULE

MAZDA

NHTSA No agency class Jul 17, 2017

FREIGHTLINER,WESTERN STAR 2018: EQUIPMENT

FREIGHTLINER,WESTERN STAR

NHTSA No agency class Jul 17, 2017

NISSAN 2007-2012: AIR BAGS:FRONTAL:DRIVER SIDE:INFLATOR MODULE

NISSAN

NHTSA No agency class Jul 16, 2017

SMART 2016: PARKING BRAKE

SMART

USDA FSIS Critical Jul 15, 2017

Marathon Enterprises Inc. Recalls Hot Dog Products Due to Possible Extranous Material Contamination

Marathon Enterprises Inc.

NHTSA No agency class Jul 14, 2017

SMART 2017: STEERING

SMART

USDA FSIS Moderate Jul 14, 2017

Custom Culinary, Inc. Recalls Chicken and Beef Products Due to Misbranding and Undeclared Allergens

Custom Culinary, Inc.

CPSC No agency class Jul 13, 2017

TJX Recalls Glass Beer Mugs Due to Burn and Laceration Hazards; Sold Exclusively at HomeGoods Stores

CPSC No agency class Jul 13, 2017

TOMY Recalls Munching Max Chipmunk Toys Due to Laceration Hazard

CPSC No agency class Jul 13, 2017

YSN Imports Recalls Refillable Propane Cylinders Due to Fire, Explosion Hazards

YSN Imports Inc., DBA Flame King, of Gardena, Calif.

NHTSA No agency class Jul 13, 2017

KENWORTH,PETERBILT 2017-2018: FUEL SYSTEM, DIESEL

KENWORTH,PETERBILT

NHTSA No agency class Jul 13, 2017

HONDA 2017: FUEL SYSTEM, GASOLINE:DELIVERY:HOSES, LINES/PIPING, AND FITTINGS

HONDA

FDA Food Moderate Jul 12, 2017

1/2" Thick Cut Beer Battered Onion Rings: ALE HOUSE BEER BATTERED STEAK CUT ONION RINGS NET WT. 10 lb (4.45 kg) - 33074

Oxford Frozen Foods Plant 1

FDA Food Moderate Jul 12, 2017

Gourmet Bay - Toasted Crumb Breaded Tilapia, 5-7 oz. (Bulk 5 lbs container) refrigerated Product Code: 7396701

Slade Gorton & Company, Inc.

FDA Food Moderate Jul 12, 2017

Don's Salads; Magnum Shrimp Salad; Net Wt. 5 lbs., MFGD by Aldon Food Corp, Schwenksville, PA 19473; Sell By: 6/7, 6/12, 6/16, 6/26; UPC: 740247006013

Aldon Food Corp. dba Don's Salads & Don's Food Products

FDA Food Moderate Jul 12, 2017

Small White Button Mushroom Regular Batter: ATLANTIC GOLD Battered Mushrooms Net Weight 5 lb (2.27 kg) - 34086; Atlantic Gold Battered Mushrooms 6 x 2 lbs 12 lbs - 34112;

Oxford Frozen Foods Plant 1

FDA Food Moderate Jul 12, 2017

go macro MACROBAR, coconut + almond butter + chocolate chips, in the following sizes: 1. Net Wt 0.9 oz / 25 G minbar, UPC 8 53555-00671 9 and 2. net Wt 2.3 oz / 65 G, UPC 8 53555-00668 9

GoMacro, Inc.

FDA Food Critical Jul 12, 2017

Taste of Inspirations; Greek Pasta Salad, Net Wt. 10 oz.; Distributed By: DZA Brands, LLC, Salisbury, NC 28147/Scarborough, ME 04074;

ASK Foods Inc

FDA Food Moderate Jul 12, 2017

5/8" Thick Cut Beer Battered Onion Rings: ALE HOUSE BEER BATTERED STEAK CUT ONION RINGS NET WT. 4/2.5 lb 10 lb (4.45 kg) - 33223; OXFORD 5/8" Beer Battered Onion Rings 4-40oz (2.5 lb) 1.13kg Packages (Net Weight 10 lb (4.54kg) - 33145; Bellissimo Beer Battered Onion Rings Net Weight 4 x 2.45 lbs 10 lbs - 33187

Oxford Frozen Foods Plant 1

FDA Food Moderate Jul 12, 2017

Finola, Style Octopus in Garlic, Product of Spain, Wild Caught, Net Weight 4.1/10oz (115g), Empacado para:/Packaged for: Bacalafoods Corp., San Juan, PR 00936-8060

Bacalafoods Corp

FDA Food Critical Jul 12, 2017

Vanilla Shortbread Collagen Protein Bite. Each Bite is packed in foil wrapper, net wt. per Bar is 0.74 oz (21g). There 15 pieces packed in a box and the net wt. is 11.10 oz (315 g). Individual Bar UPC 815709021504. Box UPC 815709021511.

Bulletproof 360 Inc

FDA Food Critical Jul 12, 2017

Robin Hood All Purpose Flour 1.8kg retial Pouch 6/1.8kg retial pouches per wholesale case

Element Food Solutions

FDA Food Critical Jul 12, 2017

Schnucks Bakery, Sliced Pudding Cake Tray, NET WT 2.00 lb (907 g)

Schnucks Markets Corporate Office

FDA Food Moderate Jul 12, 2017

Sabor Mexicano Homemade Corn Chips: Packaged in 12 oz. (9 units per case), UPC 8-53094-00417-7, and Fun size 5 oz. ( 12 units per case), UPC 8-53094-00418-4.

Sabor Mexicano

FDA Food Moderate Jul 12, 2017

Don's Salads; Chopped Herring Salad; Net Wt. 5 lbs., MFGD by Aldon Food Corp, Schwenksville, PA 19473; Sell By: 6/9, 6/11, 6/17, 6/24; UPC: 740247005023

Aldon Food Corp. dba Don's Salads & Don's Food Products

FDA Food Critical Jul 12, 2017

Fudge Brownie Collagen Protein Bite. Each Bite is packed in foil wrapper, net wt. per Bite 0.74 oz (21g). There 15 pieces packed in a box and the net wt. is 11.10 oz (315 g). Individual Bar UPC 815709021528. Box UPC 815709021535.

Bulletproof 360 Inc

FDA Food Moderate Jul 12, 2017

Gourmet Bay - Citrus Coconut Breaded Tilapia, 5-7 oz (Bulk 5 lbs) refrigerated Product Code: 7322401

Slade Gorton & Company, Inc.

FDA Food Moderate Jul 12, 2017

Finola, Style Octopus in Oil, Product of Spain, Wild Caught, Net Weight 4.1/10oz (115g), Empacado para:/Packaged for: Bacalafoods Corp., San Juan, PR 00936-8060

Bacalafoods Corp

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.