PlainRecalls

2017 Recalls

6,356 recalls · Page 41 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, NHTSA, and USDA FSIS 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 9 critical, 41 moderate, and 0 lower-severity recalls. The page references 22 distinct recalling firms operating in 6 distinct product categories, with 44 of 50 records disclosing affected-unit counts. Issuing-agency distribution on this slice leans toward FDA Devices (20), FDA Drug (19), NHTSA (6), 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, NHTSA, or USDA FSIS for the system-of-record on any specific recall. PlainRecalls indexes this archive for research and consumer awareness purposes.

FDA Drug Moderate Aug 2, 2017

MAGNESIUM Sulfate 4 g added to 100 mL 0.9% Sodium Chloride, Total Approximate Volume 108 mL (does not include mfg. overfill) Single Dose Container ba…

SCA Pharmaceuticals

FDA Drug Moderate Aug 2, 2017

PHENYLephrine HCl 10 mg in 0.9% Sodium Chloride 250 mL Bag, Preservative Free, Rx only, SCA Pharmaceuticals 8821 Knoedl Ct Little Rock, AR 72205 --- …

SCA Pharmaceuticals

FDA Drug Moderate Aug 2, 2017

morphine sulfate 1 mg per mL in 0.9% Sodium Chloride, (Total morphine Dose 100 mg/100 mL), Total Volume 100 mL Single Dose Container bag, Rx Only, SC…

SCA Pharmaceuticals

FDA Drug Moderate Aug 2, 2017

ePHEDrine Sulfate 5 mg/mL in NS 5 mL Fill in 12 mL Syringe (25 mg), Rx only, SCA Pharmaceuticals 8821 Knoedl Ct Little Rock, AR 72205 --- NDC# 70004…

SCA Pharmaceuticals

FDA Drug Moderate Aug 2, 2017

fentaNYL as citrate 5 mcg/mL in 0.9% Sodium Chloride 1 mL in Single Dose syringe, Rx only, SCA Pharmaceuticals 8821 Knoedl Ct Little Rock, AR 72205 -…

SCA Pharmaceuticals

FDA Drug Moderate Aug 2, 2017

PHENYLephrine 10 mg in 0.9% Sodium Chloride 250 mL bag, Rx only, SCA Pharmaceuticals 8821 Knoedl Ct Little Rock, AR 72205 ---- NDC# 70004-0811-59

SCA Pharmaceuticals

FDA Drug Moderate Aug 2, 2017

BUPIVacaine HCl 0.2% IN 0.9% Sodium Chloride 250 mL Bag Preservative Free (Total Dose Bupivacaine 500 mg per 250 mL), Rx only, SCA Pharmaceuticals 88…

SCA Pharmaceuticals

FDA Drug Moderate Aug 2, 2017

NORepinephrine 4 mg in 0.9% Sodium Chloride 250 mL from Stock, Rx only, SCA Pharmaceuticals 8821 Knoedl Ct Little Rock, AR 72205 --- NDC# 70004-0771-…

SCA Pharmaceuticals

FDA Drug Moderate Aug 2, 2017

BUPIVacaine HCl 0.1% PF (From 0.75%) in 0.9% Sodium Chloride, 250 mL Bag, Preservative Free (Waste From 250 mL Bag), Rx only, SCA Pharmaceuticals 882…

SCA Pharmaceuticals

FDA Drug Moderate Aug 2, 2017

Potassium Chloride 20 meq Added to Sodium Chloride 0.9% 250 mL, Rx only, SCA Pharmaceuticals 8821 Knoedl Ct Little Rock, AR 72205 --- NDC# 70004-0832…

SCA Pharmaceuticals

FDA Drug Moderate Aug 2, 2017

Potassium Chloride 40 meq Added to Sodium Chloride 0.9% 250 mL, Rx only, SCA Pharmaceuticals 8821 Knoedl Ct Little Rock, AR 72205 ---- NDC# 70004-083…

SCA Pharmaceuticals

FDA Drug Moderate Aug 2, 2017

fentaNYL 10 mcg/mL PF in Sodium Chloride 250 mL (Total Dose=2500 mcg), Rx only, SCA Pharmaceuticals 8821 Knoedl Ct Little Rock, AR 72205 --- NDC# 700…

SCA Pharmaceuticals

FDA Drug Moderate Aug 2, 2017

NORepinephrine Bitartrate 8 mg in 0.9% Sodium Chloride 250 mL, Rx only, SCA Pharmaceuticals 8821 Knoedl Ct Little Rock, AR 72205 --- NDC# 70004-0774-…

SCA Pharmaceuticals

FDA Drug Moderate Aug 2, 2017

NORepinephrine Bitartrate 16 mg in 0.9% Sodium Chloride 250 mL from Stock, Rx only, SCA Pharmaceuticals 8821 Knoedl Ct Little Rock, AR 72205 --- NDC#…

SCA Pharmaceuticals

FDA Drug Moderate Aug 2, 2017

PHENYLephrine HCl 25 mg in 0.9% Sodium Chloride 250 mL, Rx only, SCA Pharmaceuticals 8821 Knoedl Ct Little Rock, AR 72205 --- NDC# 70004-0810-40

SCA Pharmaceuticals

FDA Drug Moderate Aug 2, 2017

PHENYLephrine 100 mg in 0.9% Sodium Chloride 250 mL Bag, Rx only, SCA Pharmaceuticals 882PHENYLephrine 100 mg 1 Knoedl Ct Little Rock, AR 72205 --- …

SCA Pharmaceuticals

FDA Drug Moderate Aug 2, 2017

fentaNYL 3 mcg/mL + BUPIvacaine 0.1% in 0.9% Sodium Chloride 250 mL, Rx only, SCA Pharmaceuticals 8821 Knoedl Ct Little Rock, AR 72205 --- NDC# 70004…

SCA Pharmaceuticals

FDA Drug Moderate Aug 2, 2017

EPINEPHrine HCl 4 mg in 0.9% Sodium Chloride 250 mL, Rx only, SCA Pharmaceuticals 8821 Knoedl Ct Little Rock, AR 72205 --- NDC# 70004-0613-40

SCA Pharmaceuticals

FDA Drug Moderate Aug 2, 2017

PHENYLephrine HCl 10 mg in 0.9% Sodium Chloride, (Final Concentration = 0.1 mg per mL), Total Volume 100 mL Single Dose Container bag, Rx Only, SCA P…

SCA Pharmaceuticals

FDA Devices Moderate Aug 2, 2017

DLP Pressure Disposable Pressure Display Sets Extends the pressure line in order to reach the pressure monitoring unit during cardiopulmonary bypass…

Medtronic Perfusion Systems

FDA Devices Moderate Aug 2, 2017

STOCKERT Heater-Cooler System 3T, 120V/60 Hz

Sorin Group USA, Inc.

FDA Devices Moderate Aug 2, 2017

Smiths Medical CADD Blue-Striped IV Administration Set, REF 21-7036-01, Sterilized using ethylene oxide.

Smiths Medical ASD Inc.

FDA Devices Critical Aug 2, 2017

CS 300 Intra-Aortic Balloon Pump

Maquet Datascope Corp - Cardiac Assist Division

FDA Devices Moderate Aug 2, 2017

STOCKERT Heater-Cooler System 3T, 230 V

Sorin Group USA, Inc.

FDA Devices Moderate Aug 2, 2017

VITEK 2 Gram Negative test kits containing colistin (cs01n)

Biomerieux Inc

FDA Devices Moderate Aug 2, 2017

Medtronic Visualase(R) Cooled Laser Applicator System (VCLAS) 15MM TIP, REF 9735561, (1) Laser Diffusing Fiber - 600um Core, 15mm Tip, (1) Cooling Ca…

Medtronic Navigation, Inc.

FDA Devices Moderate Aug 2, 2017

Converters(R) Tiburon(R) Arthroscopy Drape, REF 9414, STERILE EO, Qty. 1, Cardinal Health, Waukegan, IL A surgical drape and drape accessories is …

Cardinal Health 200, LLC

FDA Devices Moderate Aug 2, 2017

Pacific Hemostasis FDP (Fibrinogen Degradation Products) Assay Kit (30 Determinations), REF/Model 100650, UDI 00845275000863, IVD; --- Fisher Diagno…

Fisher Diagnostics

FDA Devices Moderate Aug 2, 2017

DLP Antegrade/Retrograde Adapter Method for perfusion of cardioplegia alternately in either an antegrade or retrograde fashion. It is fitted with fl…

Medtronic Perfusion Systems

FDA Devices Moderate Aug 2, 2017

STOCKERT Heater-Cooler System 3T, 208V/60 Hz

Sorin Group USA, Inc.

FDA Devices Moderate Aug 2, 2017

STOCKERT Heater-Cooler System 3T, 240V/60 Hz

Sorin Group USA, Inc.

FDA Devices Moderate Aug 2, 2017

DLP Cardioplegia Adapter with Pressure Port Provides access for a pressure monitoring needle near the connection to the cardioplegia cannula. These …

Medtronic Perfusion Systems

FDA Devices Moderate Aug 2, 2017

Converters(R) Under Buttocks Drape with Fluid Control Pouch II, REF 8482, STERILE R, Qty. 1, Cardinal Health, Waukegan, IL A surgical drape and dr…

Cardinal Health 200, LLC

FDA Devices Critical Aug 2, 2017

CS 100i Intra-Aortic Balloon Pump

Maquet Datascope Corp - Cardiac Assist Division

FDA Devices Moderate Aug 2, 2017

Atrium iCAST Balloon Expandable Covered Stent; 7mm x 22mm x 120cm; Model/Part Number 85455 (Marketed in U.S. only) Atrium Advanta V12 Balloon Exp…

Atrium Medical Corporation

FDA Devices Moderate Aug 2, 2017

INVUITY(R) PhotonBlade(TM), REF PB1

Invuity, Inc.

FDA Devices Critical Aug 2, 2017

CS 100 Intra-Aortic Balloon Pump

Maquet Datascope Corp - Cardiac Assist Division

FDA Devices Moderate Aug 2, 2017

Diagnostics Ultrasound System Ultrasounds System Sonimage HS1

Konica Minolta, Inc.

FDA Devices Moderate Aug 2, 2017

Pacific Hemostasis FDP Latex Reagent, REF/Model Number 100651, UDI 00845275000870, 1 x 5 mL, IVD; --- Fisher Diagnostics, a division of Fisher Scient…

Fisher Diagnostics

CPSC Moderate Aug 2, 2017

Fred's Recalls Charcoal Grills Due to Fire Hazard

Bazhou Sanxin Steel, of China

CPSC Moderate Aug 2, 2017

Sweet Bamboo Recalls Children's Pajamas Due to Violation of Federal Flammability Standard

Sweet Bamboo, of Carlsbad, Calif.

NHTSA Critical Aug 2, 2017

JEEP 2017: ELECTRICAL SYSTEM: INSTRUMENT CLUSTER/PANEL

JEEP

CPSC Moderate Aug 1, 2017

MixBin Electronics Recalls iPhone Cases Due to Risk of Skin Irritation and Burns

MixBin Electronics LLC, of Hamilton, N.J.

CPSC Moderate Aug 1, 2017

Panelcraft Recalls Children's Building Sets Due to Choking Hazard

Panelcraft Inc., of Dearborn, Mich.

CPSC Moderate Jul 28, 2017

Nestlé Waters North America Recalls AccuPure Water Dispensers Due to Fire and Burn Hazards (Recall Alert)

Water Solutions (Hong Kong) Limited of Hong Kong

NHTSA Critical Jul 28, 2017

CHRYSLER 2017: POWER TRAIN:DRIVELINE:DIFFERENTIAL UNIT

CHRYSLER

NHTSA Critical Jul 28, 2017

BMW 2009-2018: EQUIPMENT

BMW

NHTSA Critical Jul 28, 2017

FREIGHTLINER,MERCEDES-BENZ 2012: AIR BAGS:FRONTAL:PASSENGER SIDE:INFLATOR MODULE

FREIGHTLINER,MERCEDES-BENZ

NHTSA Critical Jul 28, 2017

FREIGHTLINER,MERCEDES-BENZ 2010-2011: AIR BAGS:FRONTAL:PASSENGER SIDE:INFLATOR MODULE

FREIGHTLINER,MERCEDES-BENZ

NHTSA Critical Jul 28, 2017

DODGE,FREIGHTLINER 2007-2009: AIR BAGS:FRONTAL:PASSENGER SIDE:INFLATOR MODULE

DODGE,FREIGHTLINER

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 + USDA FSIS — consumer product, vehicle, and meat/poultry recall feeds for 2017