2017 Recalls
6,356 recalls · Page 77 of 128
2017 Recall Year Insight
Federal agencies issued 6,356 product recalls indexed by PlainRecalls in calendar year 2017. That represents about 7.57% of the 83,949 total recalls we track from 1995 through the present, and averages roughly 17.4 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 128 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 11 critical, 38 moderate, and 1 lower-severity recalls. The page references 26 distinct recalling firms operating in 5 distinct product categories, with 46 of 50 records disclosing affected-unit counts. Issuing-agency distribution on this slice leans toward FDA Devices (28), FDA Food (10), CPSC (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.
DOLPHIN INFLATION DEVICE CALIBER INFLATION DEVICE; Catalog Number: CL3030- 018SNA- 018SND 0185NA 0185ND; INTERNAL CODE NUMBER: 0185TR- 0185NA- 018SND…
PEROUSE MEDICAL
11CM ANGLE ATTACHMENT, BLACK MAX
The Anspach Effort, Inc.
Schiller AG ISA CO2 Sensor (AKA: PhaseIn Unit), Merge Part Number HW-HEMO-00001. The PhaseIn Unit is an optional accessory (sold separately) to the …
Merge Healthcare, Inc.
Dressing Rect L, P/N 02428 Product Usage: These products are sterile dressings used as an insulation barrier between the Polar Care cold therapy …
Breg Inc
eMax2 Hybrid Hand Control Product Usage: Electric system
The Anspach Effort, Inc.
Compact Speed Reducer, 60:1 Black Max
The Anspach Effort, Inc.
Electronic Foot Control with Direction Switch Product Usage: Electric system
The Anspach Effort, Inc.
10.5cm QD Angle Attachment Product Usage: Pneumatic system
The Anspach Effort, Inc.
IMRI MOTOR Product Usage: Pneumatic system
The Anspach Effort, Inc.
Foot Control, SC2100 Product Usage: Electric system
The Anspach Effort, Inc.
Accu-Chek Connect Diabetes Management App versions 2.0.0, 2.0.1 and 2.1.0 for iOS and Android Product Usage: This is a digital product available …
Roche Diabetes Care, Inc.
22CM MICRO REVISION ATTACH, BLACK MAX
The Anspach Effort, Inc.
Autolube-III with NK Product Usage: Pneumatic system
The Anspach Effort, Inc.
RENOVATION, THIN OSTEOTOME BLADE, 8 MM X 5 INCH, REF 71369408, STERILE R, QTY: (1)
Smith & Nephew, Inc.
Electronic Foot Control with Direction or Irrigation Switches Product Usage: Electric system
The Anspach Effort, Inc.
AQUIOS CL Flow Cytometer, Ref no. B30166, Software Versions 2.0 and 2.0.1 Product Usage: The AQUIOS CL Flow Cytometer is intended for use with in…
Beckman Coulter Inc.
The TM Ardis Interbody System implant is a convex, straight TLIF or PLIF device for interbody fusion of the anterior column of the spine. TM Ardis is…
Zimmer Trabecular Metal Technology, Inc.
AL-III W/ male disconnect and 30ft hose Product Usage: Pneumatic system
The Anspach Effort, Inc.
RENOVATION, THIN OSTEOTOME BLADE, 10 MM X 3 INCH, REF 71369210, STERILE R, QTY: (1)
Smith & Nephew, Inc.
RENOVATION, THIN OSTEOTOME BLADE, 10 MM X 3 INCH, REF 71369410, STERILE R, QTY: (1)
Smith & Nephew, Inc.
Adult Craniotome Product Usage: Pneumatic system
The Anspach Effort, Inc.
RENOVATION, THIN OSTEOTOME BLADE, 12 MM X 3 INCH, REF 71369212, STERILE R, QTY: (1)
Smith & Nephew, Inc.
RENOVATION, THIN OSTEOTOME BLADE, 20 MM X 3 INCH, REF 71369220, STERILE R, QTY: (1)
Smith & Nephew, Inc.
20.2cm Heavy Duty Long Heavy Short Attachment
The Anspach Effort, Inc.
5.0cm Heavy Duty Short Attachment
The Anspach Effort, Inc.
Sagittal MICRO-SAW
The Anspach Effort, Inc.
XMAX Motor (Pneumatic Drill System) Product Usage: Pneumatic system
The Anspach Effort, Inc.
Pediatric Craniotome
The Anspach Effort, Inc.
Night Lights Recalled by AM Conservation Group Due to Fire Hazard
AM Conservation Group Inc. of Charleston, S.C.
Profile Design Recalls Bicycle Handlebar Stems Due to Loss of Control and Crash Hazard
Profile Design LLC, of Carson, Calif.
Recreational Off-Highway Vehicles Recalled by American Honda Due to Risk of Injury (Recall Alert)
American Honda Motor Company Inc., of Torrance, Calif.
Snowmobiles Recalled by Polaris Due to Crash Hazard (Recall Alert)
Polaris Industries Inc., of Medina, Minn.
MERCEDES-BENZ 2017: ELECTRONIC STABILITY CONTROL (ESC)
MERCEDES-BENZ
CHEVROLET 2016-2017: AIR BAGS:FRONTAL:PASSENGER SIDE:INFLATOR MODULE
CHEVROLET
JEEP 2017: POWER TRAIN:AXLE ASSEMBLY:AXLE SHAFT
JEEP
Segway Reannounces Recall of Off-Board Chargers for Segway Personal Transporters Due to Shock Hazard (Recall Alert)
Segway Inc., of Bedford, N.H.
Springs Window Fashions Recalls Lithium Batteries Sold with Motorized Window Coverings Due to Fire and Burn Hazards (Recall Alert)
Springs Window Fashions LLC, of Middleton, Wisc. (window coverings)
Women's Scarves Recalled by DGFA Due to Violation of Federal Flammability Standard; Sold Exclusively on Amazon.com (Recall Alert)
DGFA Inc., of China
Combi USA Recalls Stroller and Car Seat Combos Due to Fall Hazard
HONDA 2015-2016: ENGINE
HONDA
Liquid Whey; Bulk.
Deutsch Kase Haus, LLC
MP MUSCLEPHARM, ASSAULT, ENERGY + STRENGTH, THE ATHLETES PRE-WORKOUT, GREEN APPLE, 11.75 OZ (O.73 LBS) (333G), Exclusively Developed & Manufactured …
Armada Nutrition
Econo, Estilo Pulpo a la Marinera, Octopus Style Marinera Sauce, Net Wt. 4oz (115g)
Supermercado Econo Inc. E
Wheat Tea Rolls, Valley Bakery, Rock Valley, IA, 12 count. UPC 290219203556, packaged in clear plastic bags
Valley Bakery Wholesalers Inc
Holstein Crimp Bread, Valley Bakery, Rock Valley, IA, 1 count. UPC 290113203607, packaged in clear plastic bags
Valley Bakery Wholesalers Inc
Cheddar cheese. All affected product private labeled for other companies. Brands: Guggisberg; Amish Classics; Dutch Farms; Banquet; Produ…
Deutsch Kase Haus, LLC
Whole Foods Market Made Right Here 6pk Banana Choc Chip Muffins, 6 pack. Net Wt. 1 lb 1 oz.
Whole Food Market
Lemongrass Satay, Net: 9oz (265gr), 12units/case and 1/2 gallon, 6 units/case
TP Food Processing Inc.
Thunder Jack Cheese sold under the following brand names: Amish Classic Firecracker & Guggisberg
Guggisberg Cheese Inc
Pepper Colby-Jack (or: Pepper Marble Jack; Lightning Jack; Thunder Jack; Firecracker; Jalapeno Jack; Jumping Jack) cheese. All affected product priv…
Deutsch Kase Haus, LLC
Nearby Recall Years
Browse recalls from adjacent calendar years to see how federal enforcement volume has shifted over time.
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
Read our methodology — how this data is sourced, computed, and verified.