PlainRecalls

2015 Recalls

8,016 recalls · Page 69 of 161

2015 Recall Year Insight

Federal agencies issued 8,016 product recalls indexed by PlainRecalls in calendar year 2015. That represents about 7.88% of the 101,704 total recalls we track from 1995 through the present, and averages roughly 22.0 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 161 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 2015.

On this page of 50 records, severity classification shows 1 critical, 49 moderate, and 0 lower-severity recalls. The page references 15 distinct recalling firms operating in 1 distinct product categories, with 50 of 50 records disclosing affected-unit counts. Issuing-agency distribution on this slice leans toward FDA Devices (50), 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 2015 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 Jul 29, 2015

iovera 155 Smart Tip; Catalog numbers:STT0412-10 and STT0412-5 (10 and 5 count respectively) iovera Smart Tips are individually packaged in Tyv…

Myoscience Inc

FDA Devices Moderate Jul 29, 2015

Perkin Elmer WIZARD2 10-detector, 1000 samples Product Code: 2470-0200, 3470-0200 The Wizard¿" gamma counter is intended to detect and count gamm…

Perkinelmer

FDA Devices Moderate Jul 29, 2015

GE Healthcare Precision RXi 23A/32A Analog System

GE Healthcare

FDA Devices Moderate Jul 29, 2015

Mermaid Medical M-Biopsy Coaxial Introducer Needle, Coaxial Needle for M-Biopsy 18Gx10cm-PRO-MAG, RX Only. Single packed device in a tyvek pouches. 1…

Mermaid Medical A/S

FDA Devices Moderate Jul 29, 2015

Flexor RTPS Guiding Sheath Product Usage: The Flexor RTPS Guiding Sheaths are intended for introduction of balloons, closed and non-tapered end c…

Cook Inc.

FDA Devices Moderate Jul 29, 2015

ATTUNE RP CR ARTICULATION SURFACE SIZE 3-8 INTENDED USE: The Tibial Articulation Surface Trial snaps together with the Shim component to function a…

DePuy Orthopaedics, Inc.

FDA Devices Moderate Jul 29, 2015

ATTUNE RP PS ARTICULATION SURFACE SIZE 3-8 INTENDED USE: The Tibial Articulation Surface Trial snaps together with the Shim component to function…

DePuy Orthopaedics, Inc.

FDA Devices Moderate Jul 29, 2015

ATTUNE CONV FB CR TB TRL SZ3 - 10 INTENDED USE: The Tibial Articulation Surface Trial snaps together with the Shim component to function as the I…

DePuy Orthopaedics, Inc.

FDA Devices Moderate Jul 29, 2015

Sureflex 910 Lithotripsy Fiber, 5x, Blue; Sure F!ex laser fibers are intended for use in laser-based surgical applications, including, but not lim…

American Medical Systems Innovation Center - Silicon Valley

FDA Devices Moderate Jul 29, 2015

Tool, Stripper W/BLD, 14S, Autoclavable; The Fiber Stripper is a tool provided for stripping the protective jacket off the end of an Endostat or S…

American Medical Systems Innovation Center - Silicon Valley

FDA Devices Moderate Jul 29, 2015

Hysto Pack, Non-sterile Part Number Description SA2059B MAJOR BASIN SA2220 HYSTO PACK SA2220A HYSTO PACK

Covidien LLC

FDA Devices Moderate Jul 29, 2015

Mini-Kits, Sterile-Kits containing the Devon Light Glove Catalog Numbers/Description 31141479 K-1842-S OR Mini Kit 31141487 K-1560-S3 OR Mini Ki…

Covidien LLC

FDA Devices Moderate Jul 29, 2015

THOMAS by Gardner Denver, MEDI-PUMP(R) Aspirator, Model 1242 Product Usage: medical aspirator

Gardner Denver Thomas Inc

FDA Devices Moderate Jul 29, 2015

Surgical Kit Sterile-Kits containing the Devon Light Glove Catalog Numbers/Description: 573326 7497-HLS Surgical Kit 573328 7437-NRF SURGICAL ASC …

Covidien LLC

FDA Devices Moderate Jul 29, 2015

THOMAS by Gardner Denver, MEDI-PUMP(R) Aspirator, Model 1240 Product Usage: medical aspirator

Gardner Denver Thomas Inc

FDA Devices Moderate Jul 29, 2015

Sureflex 550 Lithotripsy Fiber, 5x, Blue; Sure F!ex laser fibers are intended for use in laser-based surgical applications, including, but not lim…

American Medical Systems Innovation Center - Silicon Valley

FDA Devices Moderate Jul 29, 2015

Tool, Stripper W/BLD, 12S, Nonautoclavable; The Fiber Stripper is a tool provided for stripping the protective jacket off the end of an Endostat o…

American Medical Systems Innovation Center - Silicon Valley

FDA Devices Moderate Jul 29, 2015

Polaris 4.75 TI Spinal System, 4.0 x 20 MM, Closed MAS, Closed Head Multiaxial Screw, Non-Sterile, Rx Only, REF 14-583020, Biomet Spine and Bone Heal…

Biomet Spine, LLC

FDA Devices Moderate Jul 29, 2015

Delivery/C-Section, Sterile-Kits containing the Devon Light Glove Catalog Numbers/Description: 56479 7335-SMC C-Section Kit 31404851 7382-O…

Covidien LLC

FDA Devices Moderate Jul 29, 2015

Tool, Stripper W/BLD, 18S, Autoclavable; The Fiber Stripper is a tool provided for stripping the protective jacket off the end of an Endostat or S…

American Medical Systems Innovation Center - Silicon Valley

FDA Devices Moderate Jul 29, 2015

GE Healthcare Precision RXi Digital system

GE Healthcare

FDA Devices Moderate Jul 29, 2015

ATTUNE CONV RP PS TB TRL SZ10 INTENDED USE: The Tibial Articulation Surface Trial snaps together with the Shim component to function as the Inse…

DePuy Orthopaedics, Inc.

FDA Devices Moderate Jul 29, 2015

Stripper, 0.6mm Disposable EndoStat Fiber, The Fiber Stripper is a tool provided for stripping the protective jacket off the end of an Endostat o…

American Medical Systems Innovation Center - Silicon Valley

FDA Devices Moderate Jul 29, 2015

Stripper, 0.3mm Disposable EndoStat Fiber, The Fiber Stripper is a tool provided for stripping the protective jacket off the end of an Endostat o…

American Medical Systems Innovation Center - Silicon Valley

FDA Devices Moderate Jul 29, 2015

Fiber Stripper, 273¿m, Autoclavable; The Fiber Stripper is a tool provided for stripping the protective jacket off the end of an Endostat or SureF…

American Medical Systems Innovation Center - Silicon Valley

FDA Devices Moderate Jul 29, 2015

ATTUNE CONV RP CR ARTICULATION SURFACE SZ1, 2, 9, and 10 INTENDED USE: The Tibial Articulation Surface Trial snaps together with the Shim compon…

DePuy Orthopaedics, Inc.

FDA Devices Moderate Jul 29, 2015

WIZARD2 2-detector, 550 samples Product Code: 2470-0020 The Wizard¿" gamma counter is intended to detect and count gamma radiation emitted by cli…

Perkinelmer

FDA Devices Moderate Jul 29, 2015

NS-3600-B LITE GLOVE 1000/CASE -Bulk, Non-sterile Catalog Number: 571711

Covidien LLC

FDA Devices Moderate Jul 29, 2015

Tool, Stripper W/BLD, 28S, Nonautoclavable; The Fiber Stripper is a tool provided for stripping the protective jacket off the end of an Endostat o…

American Medical Systems Innovation Center - Silicon Valley

FDA Devices Moderate Jul 29, 2015

Fiber Stripper, 910¿m, Autoclavable; The Fiber Stripper is a tool provided for stripping the protective jacket off the end of an Endostat or SureF…

American Medical Systems Innovation Center - Silicon Valley

FDA Devices Moderate Jul 29, 2015

Volcano s5/s5i/CORE Intravascular Ultrasound Systems software versions 3.3 and 3.4 (with and without iFR Scout Technology) and v.3.4 software kits; …

Volcano Corporation

FDA Devices Moderate Jul 29, 2015

Head Holder shipped with Ingenuity Core 128 Computed Tomography X-ray Systems. Intended to produce cross-sectional images of the body by computer …

Philips Medical Systems (Cleveland) Inc

FDA Devices Moderate Jul 29, 2015

WIZARD2 5-detector, 550 samples Product Code: 2470-0050, 3470-0050 The Wizard¿" gamma counter is intended to detect and count gamma radiation emi…

Perkinelmer

FDA Devices Moderate Jul 29, 2015

Tool, StripperW/BLD, 10S, Nonautoclavable; The Fiber Stripper is a tool provided for stripping the protective jacket off the end of an Endostat o…

American Medical Systems Innovation Center - Silicon Valley

FDA Devices Moderate Jul 29, 2015

Fiber Stripper, 200¿m, Autoclavable; The Fiber Stripper is a tool provided for stripping the protective jacket off the end of an Endostat or SureF…

American Medical Systems Innovation Center - Silicon Valley

FDA Devices Moderate Jul 29, 2015

Sureflex 200 Lithotripsy Fiber, 5x, Blue; Sure F!ex laser fibers are intended for use in laser-based surgical applications, including, but not lim…

American Medical Systems Innovation Center - Silicon Valley

FDA Devices Moderate Jul 29, 2015

Infant Heel Warmer and Infant Gel Warmer, sold under the brand names CooperSurgical and Fisher brand as follows : CooperSurgical PN 20418 WARMGEL …

CooperSurgical, Inc.

FDA Devices Moderate Jul 29, 2015

ATTUNE CONV FB CR ARTICULATION SURFACE SZ1 INTENDED USE: The Tibial Articulation Surface Trial snaps together with the Shim component to functio…

DePuy Orthopaedics, Inc.

FDA Devices Moderate Jul 29, 2015

GE Healthcare, Precision MPi fluoroscopic imaging systems.

GE Healthcare

FDA Devices Moderate Jul 29, 2015

Sureflex 365 Lithotripsy Fiber, 5x, Blue; Sure F!ex laser fibers are intended for use in laser-based surgical applications, including, but not lim…

American Medical Systems Innovation Center - Silicon Valley

FDA Devices Moderate Jul 29, 2015

GEMINI TF 64 Slice CT/PET System. The Philips GEMINI PET/CT Imaging Systems are a family of integrated diagnostic X-ray Computed Tomography (CT) a…

Philips Medical Systems (Cleveland) Inc

FDA Devices Moderate Jul 29, 2015

GEMINI TF Ready CT/PET System. The Philips GEMINI PET/CT Imaging Systems are a family of integrated diagnostic X-ray Computed Tomography (CT) and …

Philips Medical Systems (Cleveland) Inc

FDA Devices Critical Jul 29, 2015

Various OxyTOTE Portable Oxygen System regulators, Valve Integrated Pressure Regulator, one unit per package. Product Usage: Used to dispense Ox…

Western / Scott Fetzer Company

FDA Devices Moderate Jul 29, 2015

ADVIA Centaur Tni-Ultra Assay; SMN 10317708 - 100 tests and SMN 10317709 -500 tests Product Usage: For in vitro diagnostic use in the quantitativ…

Siemens Healthcare Diagnostics, Inc

FDA Devices Moderate Jul 29, 2015

Surgical Set Up kit, Sterile-Kits containing the Devon Light Glove Catalog Numbers/Description: 31144895 7614-T4 Single Basin Set Up Kit 31144960 …

Covidien LLC

FDA Devices Moderate Jul 29, 2015

Sureflex 150 Lithotripsy Fiber, 5x, Blue; Sure F!ex laser fibers are intended for use in laser-based surgical applications, including, but not lim…

American Medical Systems Innovation Center - Silicon Valley

FDA Devices Moderate Jul 29, 2015

GEMINI LXL CT/PET System. The Philips GEMINI PET/CT Imaging Systems are a family of integrated diagnostic X-ray Computed Tomography (CT) and Posit…

Philips Medical Systems (Cleveland) Inc

FDA Devices Moderate Jul 29, 2015

Stripper, 0.2mm Disposable EndoStat Fiber, The Fiber Stripper is a tool provided for stripping the protective jacket off the end of an Endostat o…

American Medical Systems Innovation Center - Silicon Valley

FDA Devices Moderate Jul 29, 2015

Volcano s5/s5i/CORE Intravascular Ultrasound Systems software versions 3.3 and 3.4 (with and without iFR Scout Technology) and v.3.4 software kits; …

Volcano Corporation

FDA Devices Moderate Jul 29, 2015

Volcano s5/s5i/CORE Intravascular Ultrasound Systems software versions 3.3 and 3.4 (with and without iFR Scout Technology) and v.3.4 software kits; …

Volcano Corporation

Nearby Recall Years

Browse recalls from adjacent calendar years to see how federal enforcement volume has shifted over time.

Compare 2015 with 2014 →

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 2015

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 2015 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.