PlainRecalls

2021 Recall Year Insight

Federal agencies issued 5,231 product recalls indexed by PlainRecalls in calendar year 2021. That represents about 5.01% of the 104,423 total recalls we track from 1995 through the present, and averages roughly 14.3 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 105 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 2021.

On this page of 50 records, severity classification shows 11 critical, 39 moderate, and 0 lower-severity recalls. The page references 24 distinct recalling firms operating in 4 distinct product categories, with 43 of 50 records disclosing affected-unit counts. Issuing-agency distribution on this slice leans toward FDA Devices (33), FDA Food (8), NHTSA (7), 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 2021 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 Devices Moderate Oct 6, 2021

Flow sensors that may be installed in the following GEHC anesthesia machines: (1) Aestiva MRI, GTIN 0080682102339; (2) Aestiva 7900; (3) Aestiva 7100; (4) Aespire System Carestation, S/5 Protiva Config., Aespire 100 Compact Wall Mount (Aespire 7100); (5) S/5 Aespire 7900; (6) Aespire View; (7) Avance; (8) Avance CS2, GTIN 00840682102292; (9) Aisys; (10) Aisys CS2, GTIN 00840682102322; (11) Amingo; (12) 9100 NXT Config, Aelite NXT; (13) Protiva 7100;

GE Healthcare, LLC

FDA Devices Moderate Oct 6, 2021

10 drops/ml, Priming volume: 46ml, Length: 130 in.-single-use for use with the Outlook Safety Infusion System and/or Horizon NXT Pump for infusion of parenteral fluids Ref: 354216

B. Braun Medical, Inc.

FDA Devices Moderate Oct 6, 2021

The Instructions for Use (IFU) for: Carotid Patch and Gelsoft Patch vascular patches. FSN says Tapered Carotid Patch 920875t

Vascutek, Ltd.

FDA Devices Moderate Oct 6, 2021

Cardiosave Rescue Intra-Aortic Balloon Pump (IABP), Model Nos. 0998-00-0800-75, 0998-00-0800-83, 0998-00-0800-85

Datascope Corp.

FDA Devices Critical Oct 6, 2021

Omnisound Gel, 250 ml bottle and 5 L container; and EcoGel 200, 250 ml bottle; Manufactured by Eco-Med. For use in ultrasound procedures.

Accelerated Care Plus Corporation

FDA Devices Moderate Oct 6, 2021

BF-P60 OES Bronchofiberscope, Model No. BF-P60

Olympus Corporation of the Americas

FDA Devices Moderate Oct 6, 2021

PAS-PORT PROXIMAL ANASTOMOSIS SYSTEM Catalog Number: FC700SU

Aesculap Implant Systems LLC

FDA Devices Critical Oct 6, 2021

DeRoyal Procedure Packs containing Smiths Medical NORMOFLO Irrigation Warming Set

Deroyal Industries, Inc. Lafollette

FDA Devices Moderate Oct 6, 2021

Corin Trinity-i, diameter 50mm Taper Size 3, Non-Occluded Ti Plasma Shell, REF 320.03.350, Sterile, a component of the Trinity Acetabular System.

Corin Ltd

FDA Devices Moderate Oct 6, 2021

V1500HP OUTLOOK PUMP SET 118-single-use for use with the Outlook Safety Infusion System and/or Horizon NXT Pump for infusion of parenteral fluids Ref: 470025

B. Braun Medical, Inc.

FDA Devices Moderate Oct 6, 2021

OUTLOOK PUMP IV SET, 134 IN.-single-use for use with the Outlook Safety Infusion System and/or Horizon NXT Pump for infusion of parenteral fluids Ref: 477009

B. Braun Medical, Inc.

FDA Devices Moderate Oct 6, 2021

Outlook Pump Add-On Set-single use, for use with the Outlook Safety Infusion System and/or Horizon NXT Pump for infusion of parenteral fluids Ref: V7400

B. Braun Medical, Inc.

FDA Devices Moderate Oct 6, 2021

BF-Q180-AC EVIS EXERA II Bronchovideoscope, Model No. BF-Q180-AC

Olympus Corporation of the Americas

FDA Devices Moderate Oct 6, 2021

FlexoStretch Model Number: 3156057 - The combination of this products allows the user to easily adjust/control the center of gravity during lift of patient.

Hill-Rom, Inc.

FDA Devices Moderate Oct 6, 2021

VACUETTE TUBE 6 ml K2E K2EDTA 13x100 pink cap-pink ring, non-ridged

Greiner Bio-One North America, Inc.

FDA Devices Moderate Oct 6, 2021

uMI 550 System - Product Usage: intended to be operated by qualified healthcare professionals to assist in the detection, localization, diagnosis, staging, restaging, treatment planning and treatment response evaluation for diseases and disorders in, but not limit to, oncology, cardiology and neurology.

Shanghai United Imaging Healthcare Co., Ltd.

FDA Devices Moderate Oct 6, 2021

OctoStretch with Stretch Leveller - The combination of this products allows the user to easily adjust/control the center of gravity during lift of patient. Model Number: 3156056

Hill-Rom, Inc.

FDA Devices Moderate Oct 6, 2021

Corin Trinity Liner ECIMA, diameter 40mm Neutral Offset, Taper Size 4, REF 322.04.640, Sterile; and Corin Trinity Liner ECIMA, diameter 36mm Neutral 4mm EPW, Taper Size 4 (Elevated Wall), REF 322.04.936, Sterile; both are components of the Trinity Acetabular System.

Corin Ltd

FDA Devices Moderate Oct 6, 2021

PAS-PORT PROXIMAL ANASTOMOSIS DEVICE US Catalog Number: FG-000001-13

Aesculap Implant Systems LLC

FDA Devices Moderate Oct 6, 2021

AMX Navigate Mobile X-Ray System

GE Healthcare, LLC

FDA Devices Moderate Oct 6, 2021

Xcela PICC with PASV Valve Technology/Kit 5 F-55cm; (Maximum Flow Rate 3.5 mL/Sec)-indicated for short or long-term peripheral access to the central venous system for intravenous therapy, including but not limited to, the administration of fluids, medications, and nutrients; the sampling of blood; and for power injection of contrast media. Catalog Number: 60M701995

Angiodynamics Inc. (Navilyst Medical Inc.)

FDA Devices Moderate Oct 6, 2021

Corin Trinity Dual Mobility, Size 4, Dual Mobility CoCr Liner, REF 321.04.540, Sterile, and Corin Dual Mobility, Size 4 42 insert/28 head, REF 325.04.042, Sterile; both are components of the Trinity Dual Mobility System.

Corin Ltd

FDA Devices Moderate Oct 6, 2021

Corin Trinity Screw, diameter 6.5mm 35mm Length, Cancellous Bone Screw, REF 321.035, Sterile; and Corin Trinity Screw, diameter 6.5mm 50mm Length, Cancellous Bone Screw, REF 321.050, Sterile, both are components of the Trinity Acetabular System.

Corin Ltd

FDA Devices Moderate Oct 6, 2021

BF-XP160F EVIS EXERA Bronchovideoscope, Model No. BF-XP160F

Olympus Corporation of the Americas

FDA Devices Critical Oct 6, 2021

GENOSYL DS (Delivery System) console, for use as a vasodilator.

Vero Biotech, LLC

FDA Devices Moderate Oct 6, 2021

Operating room table - Product Usage: intended for use during diagnostic examinations, radiologic procedures or surgical procedures to support and position a patient.

Deerfield Imaging, Inc.

FDA Devices Moderate Oct 6, 2021

NAMIC Manifolds. (1) NAMIC Angiographic MANIFOLD, Medium Pressure, REF 64038301, UPN H965640383011, 3 Valve Manifold, Off Star Handles, Ports on Right, Rx only, Sterile; (2) NAMIC Angiographic MANIFOLD, Medium Pressure, REF 64038303, UPN H965640383031, 3 Valve Manifold, On Star Handles, Ports on Right, Rx only, Sterile; (3) NAMIC Angiographic MANIFOLD High Pressure, REF 70037200, UPN H965700372001, 2 Valve Manifold, Off Handles, Ports on Right, Rx only, Sterile; (4) NAMIC Angiog

Medline Industries Inc

FDA Devices Moderate Oct 6, 2021

Elekta Monaco - Product Usage: used to make treatment plans for patients with prescriptions for external beam radiation therapy.

Elekta Inc

FDA Devices Moderate Oct 6, 2021

OUTLOOK PUMP SET, 3 CARESITE LADS, 115 IN-single use, for use with the Outlook Safety Infusion System and/or Horizon NXT Pump for infusion of parenteral fluids Ref: 490361

B. Braun Medical, Inc.

FDA Devices Moderate Oct 6, 2021

Outlook¿ Pump 15 Drop 0.2 Micron Filtered IV Set with 2 CARESITE¿ Y-Sites: single-use for use with the Outlook Safety Infusion System and/or Horizon NXT Pump for infusion of parenteral fluids Ref: 354214

B. Braun Medical, Inc.

FDA Devices Moderate Oct 6, 2021

Outlook Pump Sets w/3 CARESITE Needle-Free Injection Sites: single-use for use with the Outlook Safety Infusion System and/or Horizon NXT Pump for infusion of parenteral fluids Material ID: 352413

B. Braun Medical, Inc.

FDA Devices Moderate Oct 6, 2021

Flow sensors kept as stand-alone user replaceable spare parts for the GEHC anethesia machines: 2089610-001 FLOW SENSOR, LEGACY VAR ORF BCG (blue, cleanable) 2089610-001-S FLOW SENSOR, LEGACY VAR ORF BCG, SERVICE (blue, cleanable) 2087640-001 FLOW SENSOR, LEGACY VAR ORF AUTOCLAVABLE BCG (gray, autoclavable) 2087640-001-S FLOW SENSOR, LEGACY VAR ORF AUTOCLAVABLE BCG, SERVICE (gray, autoclavable) 2096513-001-S FLOW SENSOR ASSEMBLY 5697309 R-FMI34109-FLOW SENSOR, LEGACY VAR ORF BCG 5697310

GE Healthcare, LLC

FDA Devices Moderate Oct 6, 2021

BF-P180 EVIS EXERA II Bronchovideoscope, Model No. BF-P180

Olympus Corporation of the Americas

CPSC No agency class Oct 6, 2021

ElliptiGO Recalls Arc Model Stand-Up Bicycles Due to Fall and Injury Hazards

CPSC No agency class Oct 6, 2021

Hobby Lobby Recalls White Wood Stools Due to Fall and Injury Hazards

NHTSA No agency class Oct 6, 2021

VOLVO 2022: POWER TRAIN:AUTOMATIC TRANSMISSION

VOLVO

NHTSA No agency class Oct 6, 2021

MERCEDES-BENZ 2021: ELECTRICAL SYSTEM:WIRING

MERCEDES-BENZ

NHTSA No agency class Oct 4, 2021

INFINITI,NISSAN 2014-2016: ENGINE AND ENGINE COOLING:ENGINE:ENGINE CONTROL MODULE (ECU/ECM):SOFTWARE

INFINITI,NISSAN

NHTSA No agency class Oct 1, 2021

MERCEDES-BENZ 2020: AIR BAGS: AIR BAG/RESTRAINT CONTROL MODULE

MERCEDES-BENZ

NHTSA No agency class Oct 1, 2021

FORD 2021: AIR BAGS:FRONTAL

FORD

NHTSA No agency class Sep 30, 2021

VOLVO 2001-2009: AIR BAGS:FRONTAL:DRIVER SIDE:INFLATOR MODULE

VOLVO

NHTSA No agency class Sep 30, 2021

FORD 2020-2021: SEATS:MID/REAR ASSEMBLY

FORD

FDA Food Moderate Sep 29, 2021

MINOR'S SEAFOOD BASE NO MSG GF 6/16 OZ (1 lb) 453 G UNITS Plastic container (pint) gluten free DISTRIBUTED BY NESTLE PROFESSIONAL NORTH AMERIC, SOLON, OH 44139

Sysco Atlanta, LLC

FDA Food Moderate Sep 29, 2021

DAIYA CHEESE VEGAN CHEDDAR STYLE SLICE 8/7.8oz Plastic bag MANUFACDTURED BY: DAIYA FOODS INC., BURNABY, BC CANADA VSA 4R4 PRODUCT OF CANADA KEEP REFRIGERATED UPC 3 08 71459 00022 1

Sysco Atlanta, LLC

FDA Food Moderate Sep 29, 2021

KEN'S STEAKHOUSE DRESSING ASIAN SESAME DRESSING 4/1gallon Plastic container Ken's Foods Inc Marlborough, MA 01752 MUST BE REFRIGERATED

Sysco Atlanta, LLC

FDA Food Moderate Sep 29, 2021

1. Dickies Seafood Cooked & Spiced Shrimp (12 oz) UPC 5240700804 Sell by 9/8/2021 & 9/12/2021. Labeled containers 2. Dickies Seafood Cooked & Spiced Shrimp (2.25 LB) UPC 5240700806 Sell by9/8/2021 & 9/12/2021.Labeled containers 3. Dickies Seafood Cooked & Spiced Shrimp (5 LB) Sell by 9/8/2021.Sold in bags over the deli counter. Unlabeled.

SSPI Mid-Atlantic, Inc

FDA Food Moderate Sep 29, 2021

GORDO'S AUTHENTIC MEXICAN RESTAURANT STYLE CHEESE DIP NET WT. 5LBS METRIC WT. 1.81 kgs (4/5lbs Plastic tub) KACHWA ENTERPRISES LAKE CITY, GEORGIA 30260 MANUFACTURED BY PLANT NO. 13-370

Sysco Atlanta, LLC

FDA Food Moderate Sep 29, 2021

IMPERIAL FRESH TOMATO ROMA DICED 3/8 TRAY 1/5lbs Plastic overwrap tray

Sysco Atlanta, LLC

FDA Food Moderate Sep 29, 2021

Phillips Majestic Blue Colossal Clawfingers 20/40 6/12 oz CANS UPC 10070057145068 & Phillips Majestic Blue Large Clawfingers 50/70 6/12oz CANS UPC 10070057145167 PASTEURIZED PREMIUM CRAB MEAT WILD CAUGHT KEEP REFRIGERATED

Sysco Atlanta, LLC

FDA Food Critical Sep 29, 2021

Golden Natural Product Inc. brand Dried Apricot Subkhon with Bone, Net Wt. 16 oz (1 lb) 454 g; and Golden Natural Product Inc. brand Dried Apricot Subkhon Jumbo, Net Wt. 16 oz (1 lb) 454 g Manufactured and Packed by: Gardencells LLC, Urgut, Samarkand region Republic of Uzbekistan; Distributed in USA by: GOLDEN NATURAL PRODUCTS INC.

Golden Natural Products

Nearby Recall Years

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

Compare 2021 with 2020 →

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 2021

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 2021 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.