PlainRecalls

2017 Recalls

7,480 recalls · Page 101 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 12 critical, 38 moderate, and 0 lower-severity recalls. The page references 26 distinct recalling firms operating in 5 distinct product categories, with 48 of 50 records disclosing affected-unit counts. Issuing-agency distribution on this slice leans toward FDA Devices (26), FDA Food (17), CPSC (5), 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 Devices Moderate Apr 19, 2017

Cataract Kit, part numbers CAT1467AM and CAT1538(B. Product packaged in a convenient manner for use in a general clinical procedure

Windstone Medical Packaging, Inc.

FDA Devices Moderate Apr 19, 2017

Eye Cataract Pack, part numbers AMS1359 and AMS1359-1 Product packaged in a convenient manner for use in a general clinical procedure

Windstone Medical Packaging, Inc.

FDA Devices Moderate Apr 19, 2017

Minor Operation Kit, part number AMS1530 Product packaged in a convenient manner for use in a general clinical procedure

Windstone Medical Packaging, Inc.

FDA Devices Moderate Apr 19, 2017

Volt Resistance Unisex Rechargeable Heated Slipper (All sizes) Deep penetrating heat garment and wraps

2k Innovations Inc.

FDA Devices Moderate Apr 19, 2017

Custom Tray, part numbers PSS1111 and PSS1111(A. Product packaged in a convenient manner for use in a general clinical procedure

Windstone Medical Packaging, Inc.

FDA Devices Moderate Apr 19, 2017

Delta, Catalog Number: MS18597 in combination with Scio, Scio Four, Scio Four Oxi plus, Scio Four Oxi, Scio Four plus. Product Usage: The device…

Draegar Medical Systems, Inc.

FDA Devices Moderate Apr 19, 2017

Sterile Handpiece Sheaths, P/N 7-796-19, included in the Accessory Packages contained in the HYFRECATOR 2000 Electrosurgical Unit (ESU) cartons, 115 …

ConMed Corporation

FDA Devices Moderate Apr 19, 2017

Centricity PACS Web Diagnostic (WebDX) by GE Healthcare Dynamic Imaging Solutions is a device that receives medical images (including mammograms) and…

Ge Medical Systems Information T

FDA Devices Moderate Apr 19, 2017

Delta XL, Catalog Number: MS18596 in combination with Scio, Scio Four, Scio Four Oxi plus, Scio Four Oxi, Scio Four plus. Product Usage: The devi…

Draegar Medical Systems, Inc.

FDA Devices Moderate Apr 19, 2017

Cobas 8100 uni-directional reformatter (BRF) module with Software Version 02-xx

Roche Diagnostics Corporation

FDA Devices Moderate Apr 19, 2017

Keystone Dental Inc. PrimaConnex Straight Implant TC, WD Internal Connection 5.0 x 11.5mm. Catalog Number(s): 15636K

Keystone Dental Inc

FDA Devices Moderate Apr 19, 2017

Eye Pack, part numbers WAL1085(B and WAL1085(C\ Product packaged in a convenient manner for use in a general clinical procedure

Windstone Medical Packaging, Inc.

FDA Devices Moderate Apr 19, 2017

TotalCare Bed Systems, Model Numbers P1900, PR1900, and U1900 with 3-Level Patient Position Monitoring and Scale Upgrade Kits, Model Numbers P1947A …

Hill-Rom, Inc.

FDA Devices Moderate Apr 19, 2017

Kappa, Catalog Number: MS18853 in combination with Scio, Scio Four, Scio Four Oxi plus, Scio Four Oxi, Scio Four plus. Catalog Number(s): MS18597/MS…

Draegar Medical Systems, Inc.

FDA Devices Moderate Apr 19, 2017

Volt Resistance Heated Neck Garment Deep penetrating heat garment and wraps

2k Innovations Inc.

FDA Devices Moderate Apr 19, 2017

Refinity Short Tip Rotational Intravascular Ultrasound (IVUS) Catheter; Product number: 400-0200.273; Catalog number 89900. Cardiovascular: Th…

Volcano Corporation

FDA Devices Moderate Apr 19, 2017

Plastic Pack, part numbers AMS1028, AMS1028(A, and WAL1189. Product packaged in a convenient manner for use in a general clinical procedure

Windstone Medical Packaging, Inc.

FDA Devices Moderate Apr 19, 2017

Refinity Rotational Intravascular Ultrasound (IVUS) Catheter; Product number: 400-0200.289; Catalog number 89800. Cardiovascular: The REFINITY…

Volcano Corporation

FDA Devices Moderate Apr 19, 2017

VIDAS Estradiol II, Ref 30431-01, 60 tests The VIDAS Estradiol II (E2 II) assay is intended for use on the instruments of the VIDAS family (VITEK Im…

BioMerieux SA

FDA Devices Moderate Apr 19, 2017

Specimen Gate Laboratory; Product Number: 5002-0180 Specimen Gate Laboratory is intended for use as a data processing software used in the storage, …

PerkinElmer Life and Analytical Sciences, Wallac, OY

FDA Devices Critical Apr 19, 2017

The Medtronic StrataMR adjustable valves and shunts are designed to provide continuous cerebrospinal fluid (CSF) flow from the ventricles of the brai…

Medtronic Neurosurgery

FDA Devices Moderate Apr 19, 2017

Volt Resistance Heated Therapy Foot Wrap Deep penetrating heat garment and wraps

2k Innovations Inc.

FDA Devices Moderate Apr 19, 2017

ViperWire Advance Peripheral Guide Wire with Flex Tip, Model No. VPR-GW-FT18. Sterilized with Ethylene Oxide. The guide wire is a smooth, stain…

Cardiovascular Systems Inc

FDA Devices Moderate Apr 19, 2017

MEDTECH ROSA Brain 3.0 The device is intended for the spatial positioning and orientation of instrument holders or tool guides to be used by neurosu…

Zimmer Biomet, Inc.

FDA Devices Moderate Apr 19, 2017

Ortho Basic Pack, part number AMS6459 Product packaged in a convenient manner for use in a general clinical procedure

Windstone Medical Packaging, Inc.

FDA Devices Moderate Apr 19, 2017

Volt Resistance Heated Lower Back Garment Deep penetrating heat garment and wraps

2k Innovations Inc.

CPSC Moderate Apr 18, 2017

Cost Plus World Market Recalls Windsor-Style Dining Chairs Due to Fall Hazard

Cost Plus Management Services Inc., of Alameda, Calif.

NHTSA Critical Apr 18, 2017

ACURA,HONDA 2017: EQUIPMENT:OTHER:LABELS

ACURA,HONDA

CPSC Moderate Apr 13, 2017

Bosch Solar Services Recalls Solar Panels Due To Fire Hazard

Bosch Solar Energy Corporation, San Mateo, Calif.

CPSC Moderate Apr 13, 2017

Polaris Recalls Ranger 900 Recreational Off-Highway Vehicles Due to Fire and Burn Hazards

Polaris Industries Inc., of Medina, Minn.

CPSC Moderate Apr 13, 2017

Polaris Recalls Sportsman All-Terrain Vehicles Due to Crash Hazard (Recall Alert)

Polaris Industries Inc., of Medina, Minn.

CPSC Moderate Apr 13, 2017

Target Recalls Water Absorbing Toys Due to Serious Ingestion Hazard

NHTSA Critical Apr 13, 2017

NISSAN 2014-2017: AIR BAGS

NISSAN

FDA Food Critical Apr 12, 2017

artisanal cheese VULTO Creamery HANDMADE CHEESE, Walton Umber, NET WT. 4 lbs

Vulto Creamery

FDA Food Moderate Apr 12, 2017

Kwei Chow brand Mustard Strip with chili in oil, net weight 7.05 Oz, sauce in glass jars, shelf stable

Kwei Chow Sauce Industry Co., Ltd.

FDA Food Moderate Apr 12, 2017

RegeneSlim

VivaCeuticals, Inc. dba Regeneca Worldwide

FDA Food Moderate Apr 12, 2017

RegeneBlend

VivaCeuticals, Inc. dba Regeneca Worldwide

FDA Food Critical Apr 12, 2017

Marketside Grab and Go Col Colby 10.8 oz Set Ups

Biery Cheese, Inc.

FDA Food Moderate Apr 12, 2017

Schlabach Amish Bakery Chocolate Chip Grand-ola Bar NET WT. 2.8 OZ (80g) UPC 0 14757 13000 2 Contains: Wheat, Tree Nuts, Dairy Ingredients: Oats, cho…

Original Amish Bakery LLC

FDA Food Critical Apr 12, 2017

artisanal cheese VULTO Creamery HANDMADE CHEESE, Blue Blais

Vulto Creamery

FDA Food Critical Apr 12, 2017

Thortons Italian Footlong 6/12 oz.

Lipari Foods, Inc.

FDA Food Critical Apr 12, 2017

Thortons Italian & Provolone 12 oz.

Lipari Foods, Inc.

FDA Food Critical Apr 12, 2017

artisanal cheese VULTO Creamery HANDMADE CHEESE, Willowemoc, NET WT. 8-10 lbs @ 10" diameter

Vulto Creamery

FDA Food Moderate Apr 12, 2017

Kwei Chow brand Mustard Bamboo Shoots with chili in oil, net weight 7.40 Oz, sauce in glass jars, shelf stable

Kwei Chow Sauce Industry Co., Ltd.

FDA Food Moderate Apr 12, 2017

Choklad Not; Milk Chocolate with hazelnut Net Wt 3.5 OZ; IKEA Produced in Spain For: IKEA Food Services, AB, Almhultsgatan 2, SE-21586 Malmo, Sw…

Ikea North America Srvcs Inc

FDA Food Critical Apr 12, 2017

DELALLO Premium Sliced HOT PEPPER CHEESE NET WT. 8 OZ. (227G) INGREDIENTS: American Cheese, Cultured Pasteurized Milk, Salt, Enzymes, Jalapeno Pepper…

Biery Cheese, Inc.

FDA Food Critical Apr 12, 2017

artisanal cheese VULTO Creamery HANDMADE CHEESE, ANDES, NET WT. 12-13 lbs

Vulto Creamery

FDA Food Moderate Apr 12, 2017

RegeneArouse

VivaCeuticals, Inc. dba Regeneca Worldwide

FDA Food Moderate Apr 12, 2017

RegeneBlast

VivaCeuticals, Inc. dba Regeneca Worldwide

FDA Food Critical Apr 12, 2017

DIETZ & WATSON Pepper Jack Cheese NET WT. 8 OZ. (227G) INGREDIENTS: Cultured Pasteurized Milk, Jalapeno Peppers, Salt, Enzymes. CONTAINS: MILK DISTR…

Biery Cheese, 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