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 4 critical, 40 moderate, and 6 lower-severity recalls. The page references 17 distinct recalling firms operating in 4 distinct product categories, with 50 of 50 records disclosing affected-unit counts. Issuing-agency distribution on this slice leans toward FDA Devices (30), FDA Drug (18), FDA Food (2), 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 Food Critical Mar 8, 2017

foxy's rocky road less travelled 1 Pint

Altijira Murray Products, LLC

FDA Food Moderate Mar 8, 2017

White Chocolate Toffee, 2.2oz pouches, 6oz pouches, 7oz boxes, one pound boxes

Bell Stone Toffee

FDA Drug Low Mar 8, 2017

Zenatane (isotretinoin) capsules, 10 mg, packaged in 30-count cartons (3 x 10 blister cards), Rx Only, Manufactured By:Cipla Limited Kurkumbh Village Pune 413802 India, Manufactured For: Dr. Reddy's Laboratories, Bachupally 500 090 India, NDC 55111-135-81

Dr. Reddy's Laboratories, Inc.

FDA Drug Critical Mar 8, 2017

Domperidone capsules 10 mg, compounded, dispensed in 60, 90, and 360 count bottles, Jeffreys Drug Store 1 North Central Ave. Canonsburg, PA

Jeffreys Drug Store

FDA Drug Low Mar 8, 2017

Zenatane (isotretinoin) capsules, 30 mg, packaged in 30-count cartons (3 x 10 blister cards), Rx Only, Manufactured By:Cipla Limited Kurkumbh Village Pune 413802 India, Manufactured For: Dr. Reddy's Laboratories, Bachupally 500 090 India, NDC 5511-113-81

Dr. Reddy's Laboratories, Inc.

FDA Drug Moderate Mar 8, 2017

CycloSPORINE Capsules, USP, 100 mg, 30 count (5x6) blister cartons, Rx only, Distributed by American Health Packaging, Columbus, OH--- NDC 68084-921-25

Amerisource Health Services

FDA Drug Moderate Mar 8, 2017

Eye Wash, 4 fl oz (118 mL) bottle, OTC, Distributed by: United Exchange Corp., 17211 Valley View Ave., Cerritos, CA 90703, Made in Korea, UPC Code: 780707005828

United Exchange Corporation

FDA Drug Low Mar 8, 2017

Salicylic Acid Cream, 6%, 400g bottle, Rx Only, Manufactured By Perrigo Yeruham, Israel 80500, Distributed By Perrigo Allegan, MI 49010, NDC 45802-806-01, UPC 3 45802-806-01 7.

L. Perrigo Company

FDA Drug Moderate Mar 8, 2017

Duopa (carbidopa and levodopa enteral suspension), 4.63 mg/20 mg per mL, 100 mL cassette, 7 cassettes per carton, Rx Only, AbbVie Inc., North Chicago, IL 60064 --- NDC 0074-3012-07

AbbVie Inc.

FDA Drug Low Mar 8, 2017

Salicylic Acid Shampoo, 6%, 177 mL bottle, Rx only, Manufactured By Perrigo Yeruham, Israel, Distributed By Perrigo Allegan, MI 49010, NDC 45802-237-01, UPC 3 45802-237-01 9.

L. Perrigo Company

FDA Drug Critical Mar 8, 2017

Nano PNC Water, packaged in amber glass bottles, Rx only, ICRPstudy.com, Immune Cellular Restoration Program.

Pacific Medical Solutions

FDA Drug Moderate Mar 8, 2017

Eye Irrigating Solution, 4 fl oz (118 mL) bottle, OTC, Distributed by: Rugby Laboratories, 31778 Enterprise Drive, Livonia, MI 48150, Made in Korea, NDC 0536-1083-97

United Exchange Corporation

FDA Drug Moderate Mar 8, 2017

Indocin (Indomethacin) suppositories, USP, 50 mg, laminate strips packed in boxes of 30, Rx only, Manufactured by: G&W Laboratories Inc. South Plainfield, NJ 07080, Distributed by Iroko Pharmaceuticals, LLC Philadelphia, PA 19112, NDC 42211-0102-43

G & W Laboratories, Inc.

FDA Drug Moderate Mar 8, 2017

Alfuzosin Hydrochloride Extended-release Tablets, 10 mg, 100-count bottles, Rx only, Distributed by: Sun Pharmaceutical Industries, Inc., Cranbury, NJ 08512; Manufactured by: Sun Pharmaceutical Ind. Ltd., Halol-Baroda Highway, Halol-389, Gujarat, India, NDC 47335-956-88.

Sun Pharmaceutical Industries, Inc.

FDA Drug Moderate Mar 8, 2017

HealthA2Z CHEWABLE Aspirin (NSAID) 81 mg, Orange Flavor, 36 Chewable Tablets, a) packaged in 36-count bottle [UPC Code 369168288362 (FP0545)], b) bulk product (6K28817), OTC, Manufactured by: Allegiant Health Deer Park, NY 11729

Allegiant Health

FDA Drug Low Mar 8, 2017

Zenatane (isotretinoin) capsules, 40 mg, packaged in 30-count cartons (3 x 10 blister cards), Rx Only, Manufactured By: Cipla Limited Kurkumbh Village Pune 413802 India, Manufactured For: Dr. Reddy's Laboratories, Bachupally 500 090 India,NDC 55111-137-81

Dr. Reddy's Laboratories, Inc.

FDA Drug Moderate Mar 8, 2017

EYE WASH, 4 fl oz. (118 mL) bottle, OTC, Distributed by: Major Pharmaceutical, 31778 Enterprise Drive, Livonia, MI 48150, Made in Korea, NDC 0904-6491-20

United Exchange Corporation

FDA Drug Critical Mar 8, 2017

EYE WASH, 4 fl oz. (118 mL) bottle, OTC, Distributed by: Major Pharmaceutical, 31778 Enterprise Drive, Livonia, MI 48150, Made in Korea, NDC 0904-6491-20

United Exchange Corporation

FDA Drug Low Mar 8, 2017

Zenatane (isotretinoin) capsules, 20 mg, packaged in 30-count cartons (3 x 10 blister cards), Rx Only, Manufactured By:Cipla Limited Kurkumbh Village Pune 413802 India, Manufactured For: Dr. Reddy's Laboratories, Bachupally 500 090 India, NDC 55111-136-81

Dr. Reddy's Laboratories, Inc.

FDA Drug Moderate Mar 8, 2017

glipiZIDE Extended-Release Tablets, 5 mg, 1000 count bottles, Rx only, Mylan Pharmaceuticals Inc., Morgantown, WV --- NDC 0378-0342-10

Mylan Pharmaceuticals Inc.

FDA Devices Moderate Mar 8, 2017

DR Systems Unity PACS software, now known as Merge Unity PACS. Product Usage: Merge Unity PACS is a medical image and information management system that allows viewing, selection, processing, printing, telecommunications, and media interchange of medical images from a variety of diagnostic imaging systems.

Merge Healthcare, Inc.

FDA Devices Moderate Mar 8, 2017

Nasal Pack, part number PSS2186

Windstone Medical Packaging, Inc.

FDA Devices Moderate Mar 8, 2017

Micropuncture Check-Flo Performer Introducer Set, Individual product is packaged in a Tyvek-film sterilizable outer pouch. Introducers are intended for introduction of balloons, closed and non-tapered end catheters or other diagnostic and interventional devices

Cook Inc.

FDA Devices Moderate Mar 8, 2017

Upper Torso Tray, part number PSS1554(B

Windstone Medical Packaging, Inc.

FDA Devices Moderate Mar 8, 2017

General Surgery Pack, part number PSS1380(A

Windstone Medical Packaging, Inc.

FDA Devices Moderate Mar 8, 2017

Minor/General/Ortho Pack, part number PSS3258(B

Windstone Medical Packaging, Inc.

FDA Devices Moderate Mar 8, 2017

Surgical Pack, part number PSS3540(A

Windstone Medical Packaging, Inc.

FDA Devices Moderate Mar 8, 2017

Major Pack (1345), part number AMS6565

Windstone Medical Packaging, Inc.

FDA Devices Moderate Mar 8, 2017

Ortho Pack, part number PSS3466(A

Windstone Medical Packaging, Inc.

FDA Devices Moderate Mar 8, 2017

Orbitofacial Pack, part number AMS5850(A

Windstone Medical Packaging, Inc.

FDA Devices Moderate Mar 8, 2017

Knee Pack, part number AMS4211

Windstone Medical Packaging, Inc.

FDA Devices Moderate Mar 8, 2017

Transvaginal Pack, part number CMP1767

Windstone Medical Packaging, Inc.

FDA Devices Moderate Mar 8, 2017

Major Kit, part number PHC1307(A

Windstone Medical Packaging, Inc.

FDA Devices Moderate Mar 8, 2017

Total Hip Pack, part number PSS2956

Windstone Medical Packaging, Inc.

FDA Devices Moderate Mar 8, 2017

Laparotomy Pack, part number 006268-9 Laparotomy Pack, part number AMS4418(A Laparotomy Pack, part number PSS2190(A

Windstone Medical Packaging, Inc.

FDA Devices Moderate Mar 8, 2017

Laparoscopy Pack (1184), part number AMS6562

Windstone Medical Packaging, Inc.

FDA Devices Moderate Mar 8, 2017

Vascular Pack, part number AMS4030 Vascular Pack, part number AMS4030(A

Windstone Medical Packaging, Inc.

FDA Devices Moderate Mar 8, 2017

HSG Pack, part number PSS3287

Windstone Medical Packaging, Inc.

FDA Devices Moderate Mar 8, 2017

Basic Setup Tray, part number AMS6414

Windstone Medical Packaging, Inc.

FDA Devices Moderate Mar 8, 2017

Newport Coast Basic Pack, part number 007484-1

Windstone Medical Packaging, Inc.

FDA Devices Moderate Mar 8, 2017

Arthroscopy Pack, part number AMS6559

Windstone Medical Packaging, Inc.

FDA Devices Moderate Mar 8, 2017

General Pack, part number AMS2967(A General Pack, part number AMS3239(A General Pack, part number AMS3709(B General Pack, part number AMS5341 General Pack, part number AMS5694

Windstone Medical Packaging, Inc.

FDA Devices Moderate Mar 8, 2017

TriForce Peripheral Crossing Set, Individual product is packaged in a Tyvek-film sterilizable outer pouch. The TriForce Peripheral Crossing Set is intended to be percutaneously introduced into blood vessels and support a wire guide while performing percutaneous peripheral interventions. This device is also intended for injection of radiopaque contrast media for the purpose of angiography.

Cook Inc.

FDA Devices Moderate Mar 8, 2017

Siemens ADVIA Centaur Systems Calibrator A Kits, Cat No. 04800646, SMN 10285903 (2 pack)Cat No. 04800735, SMN 10285904 (6 pack) Cat No. 04800840, SMN 10285905 (6 pack - REF)

Siemens Healthcare Diagnostics, Inc

FDA Devices Moderate Mar 8, 2017

C-Tray Pack, part number PSS2707(A

Windstone Medical Packaging, Inc.

FDA Devices Moderate Mar 8, 2017

Basic Pack, part number AMS1868(B Basic Pack, part number AMS2608(A Basic Pack, part number AMS3861 Basic Pack, part number AMS4309 Basic Pack, part number PSS1833 Basic Pack, part number PSS1833(A Basic Pack, part number PSS1848(A

Windstone Medical Packaging, Inc.

FDA Devices Moderate Mar 8, 2017

Major Laparotomy Pack - NS, part number AMS4347

Windstone Medical Packaging, Inc.

FDA Devices Moderate Mar 8, 2017

Plastic Pack, part number PSS2462 Plastic Pack, part number PSS3319 Plastic Pack, part number PSS3319(A

Windstone Medical Packaging, Inc.

FDA Devices Moderate Mar 8, 2017

Custom Venous Kit, part number TVS4024(C

Windstone Medical Packaging, Inc.

FDA Devices Moderate Mar 8, 2017

D & C Kit, part number CMP1466(A

Windstone Medical Packaging, 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.