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 1 critical, 49 moderate, and 0 lower-severity recalls. The page references 13 distinct recalling firms operating in 2 distinct product categories, with 50 of 50 records disclosing affected-unit counts. Issuing-agency distribution on this slice leans toward FDA Devices (49), FDA Drug (1), 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 Drug Moderate Nov 29, 2017

Extra Strength Naturally HL Hemorrhoid Numbing Spray with Lidocaine, (lidocaine HCL 4%), 1/2 oz Spray (NDC 69804-015-08), 1 oz Spray (NDC 69804-015-07), 2 oz Spray (NDC 69804-015-01) and 4 oz Spray (NDC 69804-015-04) bottles, Manufactured by Pain Relief Naturally, www.Naturally HL.com

Ridge Properties, LLC

FDA Devices Moderate Nov 29, 2017

Optetrak Constrained Condylar Offset Screw, Size AA, Ref 208-04-70, Sterile, RX. .

Exactech, Inc.

FDA Devices Moderate Nov 29, 2017

ROSA Surgical Device 2.5.8, a computer-controlled electromechanical arm to guide standard neurosurgical instruments.

Zimmer Biomet, Inc.

FDA Devices Moderate Nov 29, 2017

Transfer/Gait Belt, Plastic, Wipeable, packaged in plastic bag, 36 plastic bags per box.

Medline Industries Inc

FDA Devices Moderate Nov 29, 2017

Optetrak Offset Tibial Tray and Screws, Size 4F/4T, Beta, Ref 208-04-44, Sterile, RX. .

Exactech, Inc.

FDA Devices Moderate Nov 29, 2017

Optetrak Constrained Condylar Offset Screw, Size FF, Ref 208-04-74, Sterile, RX.

Exactech, Inc.

FDA Devices Moderate Nov 29, 2017

Optetrak Constrained Condylar Offset Screw, Size EE, Ref 208-04-73, Sterile, RX.

Exactech, Inc.

FDA Devices Moderate Nov 29, 2017

ARCHITECT c4000 part number 02P24; ARCHITECT c8000 part number 01G06; ARCHITECT c16000 part number 03L77 Clinical Chemistry systems.

Abbott Laboratories, Inc

FDA Devices Moderate Nov 29, 2017

Medtronic MiniMed(TM) Pro-set(TM) (MMT-280, 281)

Medtronic Inc.

FDA Devices Moderate Nov 29, 2017

Optetrak Offset Tibial Tray and Screws, Size 5F/5T, Beta, Ref 208-04-54, Sterile, RX.

Exactech, Inc.

FDA Devices Moderate Nov 29, 2017

Halyard Closed Suction System for Adults, 14 F, T-Piece, Wet Pak. 12 or 6 vials per kit, 20 kits per case.

Halyard Health, Inc

FDA Devices Moderate Nov 29, 2017

Optetrak Offset Tibial Tray and Screws, Size 1F/1T & 2F/1T, Beta, Ref 208-04-22, Sterile, RX.

Exactech, Inc.

FDA Devices Moderate Nov 29, 2017

Optetrak Constrained Condylar Offset Screw, Size GG, Ref 208-04-75, Sterile, RX.

Exactech, Inc.

FDA Devices Moderate Nov 29, 2017

ROSA BRAIN 3.0.0

Zimmer Biomet, Inc.

FDA Devices Moderate Nov 29, 2017

Optetrak Offset Tibial Tray and Screws, Size 5F/4T, Alpha, Ref 208-04-51, Sterile, RX.

Exactech, Inc.

FDA Devices Moderate Nov 29, 2017

Halyard Closed Suction System for Adults, 14 F, DSE, Wet Pak. 12 or 6 vials per kit, 20 kits per case.

Halyard Health, Inc

FDA Devices Moderate Nov 29, 2017

Optetrak Offset Tibial Tray and Screws, Size 5F/4T, Beta, Ref 208-04-52, Sterile, RX.

Exactech, Inc.

FDA Devices Moderate Nov 29, 2017

Halyard Closed Suction System for Adults with BALLARD Technology WET PAK. 12 saline vials per kit, 20 kits per case.

Halyard Health, Inc

FDA Devices Moderate Nov 29, 2017

3M Bair Hugger(TM) Normothermia System, Temperature Monitoring System Sensors Model 360 (Part Number 36000)

3M Company - Health Care Business

FDA Devices Moderate Nov 29, 2017

Optetrak Constrained Condylar Offset Screw, Size RR, Ref 208-04-82, Sterile, RX.

Exactech, Inc.

FDA Devices Moderate Nov 29, 2017

Regard Custom Surgical Pack Packs contain surgical instruments and accessories intended for use during a surgical procedure.

Resource Optimization & Innovation Llc

FDA Devices Moderate Nov 29, 2017

Halyard Turbo-Cleaning Closed Suction System for Adults, 14 F, T-Piece, Wet Pak. 12 vials per kit, 20 kits per case.

Halyard Health, Inc

FDA Devices Moderate Nov 29, 2017

Optetrak Constrained Condylar Offset Screw, Size KK, Ref 208-04-78, Sterile, RX.

Exactech, Inc.

FDA Devices Moderate Nov 29, 2017

Sensicare Green Surgical Glove, PI, LF, PF. Packaged in a poly/poly peel pouch with Sunoco films, sterile. Surgical glove.

Medline Industries Inc

FDA Devices Moderate Nov 29, 2017

Optetrak Constrained Condylar Offset Screw, Size JJ, Ref 208-04-77, Sterile, RX.

Exactech, Inc.

FDA Devices Moderate Nov 29, 2017

Optetrak Constrained Condylar Offset Screw, Size MM, Ref 208-04-80, Sterile, RX.

Exactech, Inc.

FDA Devices Moderate Nov 29, 2017

SURPLUG MICRO CONNECTOR Item No. 066-C3352; 111" (282 cm) Appx 13.9 ml, 15 Drop Admin Set w/3-Way Stopcock, 1 Ext, Luer Slip Item No. B30167; 32" Transfer Set w/3-Way Stopcock, Clamp, Rotating Luer Item No. B30243; 10" Ext Set w/Remv 3-Way Stopcock w/MicroClave, Clamp, Rotating Luer Item No. B33084; 3-Way High Flow Stopcock w/Rotating Luer Item No. B4020; 38" Non-DEHP Smallbore Ext Set w/2 T-Connectors/Inj Sites, Remv 3-Way Stopcock, 2 Clamps, Luer Slip Item No. B4054; 300" Ext Set w

ICU Medical, Inc.

FDA Devices Moderate Nov 29, 2017

ROSA Brain 3.0.0 Usage: The device is intended for the spatial positioning and orientation of instrument holders or tool guides to be used by neurosurgeons to guide standard neurosurgical instruments (biopsy needle, stimulation or recording electrode, endoscope). The device is indicated for any neurosurgical procedure in which the use of stereotactic surgery may be appropriate.

Zimmer Biomet, Inc.

FDA Devices Moderate Nov 29, 2017

Halyard Closed Suction System for Adults, 14 F, Elbow, Directional Tip, Wet Pak. 12 vials per kit, 20 kits per case.

Halyard Health, Inc

FDA Devices Moderate Nov 29, 2017

Optetrak Offset Tibial Tray and Screws, Size 4F/4T, Alpha, Ref 208-04-43, Sterile, RX.

Exactech, Inc.

FDA Devices Moderate Nov 29, 2017

Optetrak Offset Tibial Tray and Screws, Size 3F/2T, Beta, Ref 208-04-32, Sterile, RX.

Exactech, Inc.

FDA Devices Moderate Nov 29, 2017

Optetrak Offset Tibial Tray and Screws, Size 1F/1T & 2F/1T, Alpha, Ref 208-04-21, Sterile, RX.

Exactech, Inc.

FDA Devices Moderate Nov 29, 2017

Syngo.plaza, Picture Archiving and Communications System(PACS), Model 10863171 Syngo.plaza is a Picture Archiving and Communication System (PACS) intended to display, process, read, report, communicate, distribute, store and archive digital medical images. It supports the physician in diagnosis and treatment planning. Syngo.plaza also supports storage and archiving of DICOM Structured reports. In a comprehensive imaging syngo.plaza integrates Hospital/Radiology Information Systems (HIS/RIS)

Siemens Medical Solutions USA, Inc

FDA Devices Moderate Nov 29, 2017

NOVAPLUS* Endotracheal WET PAK* Closed Suction System for Adults with BALLARD* Technology, Double Swivel Elbow, 14 F. 6 vials per kit, 20 kits per case.

Halyard Health, Inc

FDA Devices Moderate Nov 29, 2017

Tissu-Trans Filtron 1000 Catalog Number 3-TT-FILTRON 1000. Used for fat transfer and liposuction.

Shippert Medical Technologies

FDA Devices Moderate Nov 29, 2017

Optetrak Offset Tibial Tray and Screws, Size 3F/2T, Alpha, Ref 208-04-31, Sterile, RX.

Exactech, Inc.

FDA Devices Moderate Nov 29, 2017

ROSA Surgical Device 2.5.8 It is intended to be used in the operating room for the spatial positioning and orientation of an instrument holder or tool guide. Guidance is based on a pre-operative plan developed with three-dimensional imaging software, and uses fiducial markers or optical registration. The system is intended for use by neurosurgeons to guide standard neurosurgical instruments. It is indicated for any neurosurgical condition in which the use of stereotactic surgery may be appr

Zimmer Biomet, Inc.

FDA Devices Moderate Nov 29, 2017

Optetrak Offset Tibial Tray and Screws, Size 4F/3T, Alpha, Ref 208-04-41, Sterile, RX.

Exactech, Inc.

FDA Devices Moderate Nov 29, 2017

Optetrak Offset Tibial Tray and Screws, Size 1DeltaF/1T, Alpha, Ref 208-04-13, Sterile, RX.

Exactech, Inc.

FDA Devices Moderate Nov 29, 2017

Optetrak Constrained Condylar Offset Screw, Size PP, Ref 208-04-81, Sterile, RX.

Exactech, Inc.

FDA Devices Moderate Nov 29, 2017

Optetrak Offset Tibial Tray and Screws, Size 4F/3T, Beta, Ref 208-04-42, Sterile, RX.

Exactech, Inc.

FDA Devices Moderate Nov 29, 2017

Optetrak Offset Tibial Tray and Screws, Size 1DeltaF/0T, Alpha, Ref 208-04-11, Sterile, RX.

Exactech, Inc.

FDA Devices Moderate Nov 29, 2017

MEDLINE DOUBLE SWIVEL CLOSED SUCTION CATHETER, 21.3 in (54 cm) FOR ENDOTRACHEAL TUBE, 12 Fr, REF DYNCSDS12, 1 Each, Sterile

Medline Industries Inc

FDA Devices Moderate Nov 29, 2017

Optetrak Constrained Condylar Offset Screw, Size LL, Ref 208-04-79, Sterile, RX.

Exactech, Inc.

FDA Devices Moderate Nov 29, 2017

Optetrak Offset Tibial Tray and Screws, Size 1DeltaF/0T, Beta, Ref 208-04-12, Sterile, RX.

Exactech, Inc.

FDA Devices Critical Nov 29, 2017

Arkon Anesthesia Delivery System, Model 99999, and software version 2.61 and upgrade kit 050-9043-00 Rev G. The Spacelabs Arkon Anesthesia Workstation is intended for use in the hospital environment and operating room. It may be used for the delivery of oxygen, air and nitrous oxide in a controlled manner to various patient breathing circuits with or without the use of mechanical ventilator, and may be used for the delivery of anesthetic vapor by use of a dismountable vaporizer. The device i

Spacelabs Healthcare, Ltd.

FDA Devices Moderate Nov 29, 2017

Optetrak Constrained Condylar Offset Screw, Size BB, Ref 208-04-71, Sterile, RX.

Exactech, Inc.

FDA Devices Moderate Nov 29, 2017

Optetrak Constrained Condylar Offset Screw, Size DD, Ref 208-04-72, Sterile, RX.

Exactech, Inc.

FDA Devices Moderate Nov 29, 2017

Halyard Turbo-Cleaning Closed Suction System for Adults, 14 F, DSE, MDI, Wet Pak. 12 vials per kit, 20 kits per case.

Halyard Health, Inc

FDA Devices Moderate Nov 29, 2017

Transfer/Gait Belt, Plastic, Wipeable, packaged in plastic bag, 36 plastic bags per box.

Medline Industries 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: 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.