The Recall Desk

Hazard

Injury recalls

1,366 recalls in our database tag this hazard, drawn from FDA, USDA FSIS, CPSC, and NHTSA source notices.

What the numbers show

Total
1,366
Critical
6
Severe
415
Most recent
2026-09-03

Of the 1,366 injury recalls we have scored against our rubric, 6 (0%) are Critical — deaths or serious injuries reported, or the agency’s own highest classification — and 415 (30%) are Severe.

About this hazard tag

Hazard tags are short, machine-readable labels we attach to every recall to make cross-cutting queries possible — “all injury recalls regardless of agency”, “all listeria recalls in California”, “all airbag recalls in 2025”. The tags are extracted from each recall’s source text during the LLM rewrite step and validated against a fixed schema.

A recall can carry multiple tags — a Listeria recall might also be tagged ready-to-eat and undeclared-allergen. Use the full-text search if you want to combine hazard tags with brand or category filters.

751–775 of 1366

  • SevereNHTSA·16V886000·2016-12-09

    Micro Bird Recalls 2015-2016 T-Series School Buses for Lift Interlock Defect

    Micro Bird is recalling 2015-2016 T-Series school buses because the wheelchair lift interlock can be deactivated, allowing the bus to be driven with the lift open or deployed.

    Product
    MICRO BIRD — MICRO BIRD T-SERIES SCHOOL BUS
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16V844000·2016-11-21

    GM Recalls 2016 Buick Cascada for Power Window Safety Standard Violation

    General Motors is recalling 2016 Buick Cascada vehicles because an incorrect roof control module may allow windows to close automatically or remotely, increasing injury risk.

    Product
    BUICK — BUICK CASCADA
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0415-2017·2016-11-16

    Fruit 66 Mixed Berry Juice Recalled Due to Swelling and Lid Pop-Off Risk

    1 Epic, LLC is recalling specific lots of Fruit 66 Mixed Berry juice because can swelling may cause lids to pop off, posing an injury risk.

    Product
    Fruit 66 Mixed Berry, 8 FL OZ (240 mL) 100% Juice Non-Carbonated. Flavored 100% Juice Blend from concentrate with other natural Flavors and added Ingredients. UPC 98341-00117.
    Category
    Food
    Distribution
    14 states
  • HighFDA (Food)·F-0417-2017·2016-11-16

    Fruit 66 Tropical Punch Recalled Due to Swelling Cans

    1 Epic, LLC is recalling specific lots of Fruit 66 Tropical Punch because swelling cans may cause lids to pop off, posing an injury risk.

    Product
    Fruit 66 Tropical Punch, 8 FL OZ (240 mL) 100% Juice Non-Carbonated. Flavored 100% Juice Blend from concentrate with other natural Flavors and added Ingredients. UPC 98341-00108.
    Category
    Food
    Distribution
    14 states
  • HighNHTSA·16V829000·2016-11-16

    Mercedes-Benz Recalls S-Class Vehicles for Seat Belt Extender Defect

    Mercedes-Benz is recalling 672 S-Class vehicles because seat belt extenders may not retract or may break in a crash, increasing injury risk.

    Product
    MERCEDES-BENZ — MERCEDES-BENZ AMG S65, S65 AMG, AMG S63, S550
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighFDA (Food)·F-0416-2017·2016-11-16

    Fruit 66 Strawberry Melon Juice Recalled Due to Swelling Cans

    1 Epic, LLC is recalling specific lots of Fruit 66 Strawberry Melon juice because swelling cans may cause lids to pop off, posing an injury risk.

    Product
    Fruit 66 Strawberry Melon, 8 FL OZ (240 mL) 100% Juice Non-Carbonated. Flavored 100% Juice Blend from concentrate with other natural Flavors and added Ingredients. UPC 98341-00116.
    Category
    Food
    Distribution
    14 states
  • HighFDA (Food)·F-0418-2017·2016-11-16

    Fruit 66 Passion Fruit Mango Juice Recalled for Swelling Cans

    1 Epic, LLC is recalling specific lots of Fruit 66 Passion Fruit Mango juice because swelling cans may cause lids to pop off, posing an injury risk.

    Product
    Fruit 66 Passion Fruit Mango, 8 FL OZ (240 mL) 100% Juice Non-Carbonated. Flavored 100% Juice Blend from concentrate with other natural Flavors and added Ingredients. UPC 98341-00109.
    Category
    Food
    Distribution
    14 states
  • HighNHTSA·16V823000·2016-11-15

    KZRV Recalls 2015 Trailers Due to Ladder Hinge Separation Risk

    KZRV is recalling 2015 Venom, Inferno, Sportsmen, Sportster, MXT, and SportTrek trailers because aluminum ladder hinges may separate, causing the ladder to fall and increasing injury risk.

    Product
    KZRV — KZRV SPORTSTER, VENOM, SPORTSMEN, MXT
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16V828000·2016-11-15

    Forest River Recalls Motorhomes and Toyhaulers Due to Ladder Hinge Defect

    Forest River is recalling specific 2013-2017 motorhomes and toyhaulers because aluminum ladder hinges may separate, causing the ladder to fall and increasing injury risk.

    Product
    FOREST RIVER — FOREST RIVER, PALOMINO, PRIME TIME FR3, COLUMBUS, XLR, SPARTAN
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16V825000·2016-11-15

    Keystone RV Recalls Fifth Wheels Due to Ladder Hinge Defect

    Keystone RV is recalling 2015-2016 fifth wheels because aluminum ladder hinges may separate, causing the ladder to fall and increasing injury risk.

    Product
    KEYSTONE — KEYSTONE, DUTCHMEN CARBON, FUZION, RAPTOR, VOLTAGE
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16V821000·2016-11-14

    Cruiser RV Recalls Stryker Toy Haulers Due to Ladder Hinge Defect

    Cruiser RV is recalling 2015-2016 Stryker toy haulers because aluminum ladder hinges may separate, causing the ladder to fall and increasing injury risk.

    Product
    CRUISER RV — CRUISER RV STRYKER TOY
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16V818000·2016-11-14

    Highland Ridge RV Recalls 2016 Highlanders Due to Ladder Hinge Defect

    Highland Ridge RV is recalling 61 model year 2016 Highlander travel trailers because aluminum ladder hinges may separate, causing the ladder to fall and increasing injury risk.

    Product
    HIGHLAND RIDGE FW — HIGHLAND RIDGE FW HIGHLANDER
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • HighNHTSA·16V805000·2016-11-04

    Terex Recalls 2009-2014 TC and TCX Trucks for Wiring Defect

    Terex is recalling 2009-2014 TC and TCX hybrid electric trucks because improper wiring may cause the aerial boom to move unintentionally, increasing the risk of injury.

    Product
    TEREX — TEREX TC, TCX
    Category
    Vehicle
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0096-2017·2016-11-02

    Roche Recalls cobas 6000 Series Analyzers Due to Sharp Edge Injury Risk

    Roche is recalling cobas 6000 Series analyzers because the sharp edge of the sample rack tray center guide rail caused four reported injuries.

    Product
    cobas 6000 Series system c6000, Chemistry (Photometric, Discrete), for clinical Use. Modular e601: Immunoassay Analyzer Product Usage: The cobas p501/p701 instrument stores primary and secondary sample tubes. The tubes are stored in a controlled, refrigerated sample store. A
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0105-2017·2016-11-02

    Roche Recalls cobas 8000 Sorting System Modules Due to Injury Reports

    Roche is recalling 9,014 cobas 8000 Sorting System calculator/data processing modules after four reports of injury caused by a sharp edge on the sample rack tray.

    Product
    RSD 800 Sorting System calculator/data processing module, for clinical use Product Usage: The cobas 8000 Modular Analyze Series is a fully automated system for Clinical chemistry analysis, intended for the in vitro qualitative and quantitative determination of analytes in bo
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0107-2017·2016-11-02

    Roche Recalls cobas p 512 Pre-Analytical Instrument Due to Sharp Edge Injury Reports

    Roche is recalling 9,014 cobas p 512 Pre-Analytical Instruments after four reports of injury caused by a sharp edge on the sample rack tray.

    Product
    cobas p 512 Pre-Analytical Instrument calculator/data processing module, for clinical use Product Usage: The cobas 6800/8800 systems support an automated and integrated workflow to run Polymerase Chain Reaction (PCR) based Nucleic Acid Testing (NAT) to be applied in diagnost
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0098-2017·2016-11-02

    Roche Modular Pre Analytics EVO/Plus Recall for Sharp Edge Injury Risk

    Roche is recalling Modular Pre Analytics EVO/Plus systems because a sharp edge on the sample rack tray caused four reported injuries.

    Product
    Modular Pre Analytics ( EVO/Plus) Product Usage: The RSD 800A is a computer-controlled stand-online system for decapping, aliquoting and sorting of primary tubes and for producing and sorting bar coded secondary tubes.. The system operates with an online connection to the hos
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0104-2017·2016-11-02

    Roche RSD 800A Aliquoting System Recalled Due to Sharp Edge Injury Reports

    Roche is recalling 9,014 RSD 800A Aliquoting System calculator/data processing modules because four reports of injury were received from the sharp edge of the sample rack tray.

    Product
    RSD 800A Aliquoting System calculator/data processing module, for clinical use Product Usage: The Roche/Hitachi MODULAR Analytics System is a fully automated, random-access, software-controlled system for immunoassay and photometric analysis intended for qualitative and quan
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0106-2017·2016-11-02

    Roche cobas p 612 Pre-Analytical Instrument Recall for Sharp Edge Injury

    Roche is recalling cobas p 612 Pre-Analytical Instruments because the sharp edge of the sample rack tray center guide rail caused four reported injuries.

    Product
    cobas p 612 Pre-Analytical Instrument calculator/data processing module, for clinical use Product Usage: The cobas 6000 series is a fully automated, random-access, software-controlled system for immunoassay and photometric analysis intended for qualitative and quantitative i
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0102-2017·2016-11-02

    Roche Recalls cobas p 501 Post-Analytical Units Due to Sharp Edges

    Roche is recalling 9,014 cobas p 501 Post-Analytical Units because a sharp edge on the sample rack tray caused four reported injuries.

    Product
    cobas p 501 Post-Analytical Unit calculator/data processing module, for clinical use Product Usage: The MODULAR PRE-ANALYTICS system is a fully automated system for sample pre-processing, including centrifuging, aliquoting, and barcode labeling, prior to analysis by MODULAR
    Category
    Medical Device
    Distribution
    Distributed nationwide
  • SevereFDA (Devices)·Z-0101-2017·2016-11-02

    Roche Recalls cobas p 701 Post-Analytical Units Due to Sharp Edges

    Roche is recalling 9,014 cobas p 701 Post-Analytical Units because a sharp edge on the sample rack tray caused four reported injuries.

    Product
    cobas p 701 Post-Analytical Unit calculator/data processing module, for clinical use Product Usage: The URISYS 2400 Analyzer is a fully automated urinalysis system intended for in vitro qualitative or semi-quantitative determination of urine analytes, including pH, leukocyte
    Category
    Medical Device
    Distribution
    Distributed nationwide