Home › Latest Recalls

Recently reported

Latest U.S. Recalls

Browse the newest complete recall records currently stored from FDA enforcement reports and NHTSA vehicle campaigns. “Latest” refers to the newest source-dated record in this database, not the timestamp of our last API check.

63,677published records in database

4recall categories represented

Oct 25, 2018newest stored source record

Latest records

Latest recalls — page 1335

The newest recall records with useful source details are listed here.

VehicleOct 25, 2018

Toyota 4Runner labels recall — NHTSA campaign 18V753000

Southeast Toyota Distributors, LLC (SET) is recalling certain 2017-2019 Toyota 4Runner vehicles that SET modified to be equipped with a TRD wheel package. The Gross Vehicle Weight Rating…

labelsSoutheast Toyota Distributors, LLC

Medical DeviceOct 24, 2018

Zimmer Biomet Affixus Hip Fracture Nail Right 125 13 mm x 360 mm, Item Number 814313360 recall — FDA Z-0142-2019

There were complaints indicating that when the product was opened in surgery, the sterile packaging was already open.

Class IIFDA: TerminatedZimmer Biomet, Inc.

Medical DeviceOct 24, 2018

Zimmer Biomet Affixus Hip Fracture Nail Left 125 9 mm x 320 mm, Item Number 814409320 recall — FDA Z-0147-2019

There were complaints indicating that when the product was opened in surgery, the sterile packaging was already open.

Class IIFDA: TerminatedZimmer Biomet, Inc.

Medical DeviceOct 24, 2018

Zimmer Biomet Affixus Hip Fracture Nail 125 9 mm x 165 mm, Item Number 816709165 Product recall — FDA Z-0169-2019

There were complaints indicating that when the product was opened in surgery, the sterile packaging was already open.

Class IIFDA: TerminatedZimmer Biomet, Inc.

Medical DeviceOct 24, 2018

Zimmer Biomet Affixus Hip Fracture Nail Right 125 13 mm x 300 mm, Item Number 814313300 recall — FDA Z-0141-2019

There were complaints indicating that when the product was opened in surgery, the sterile packaging was already open.

Class IIFDA: TerminatedZimmer Biomet, Inc.

Medical DeviceOct 24, 2018

Zimmer Biomet Affixus Hip Fracture Nail Left 130 9 mm x 360 mm, Item Number 814609360 recall — FDA Z-0164-2019

There were complaints indicating that when the product was opened in surgery, the sterile packaging was already open.

Class IIFDA: TerminatedZimmer Biomet, Inc.

Medical DeviceOct 24, 2018

GE Medical Systems GE Healthcare MRI Systems, Software Version 15.x or HD 16 sold under the recall — FDA Z-0112-2019

The latest on-site software version may not have been reinstalled at some sites after service activities were performed resulting in images possibly flipped left/right and/or there can be…

Class IIFDA: TerminatedGE Medical Systems, LLC

Medical DeviceOct 24, 2018

AS Software AS-OBGYN Information System version 7.824.x recall — FDA Z-0118-2019

Any change made to current ultrasound machine software or hardware upgrades, adding or modifying custom fields, or adding a new Ultrasound Machine, must be tested prior to the use in…

Class IIFDA: TerminatedAS Software, Inc.

Medical DeviceOct 24, 2018

Zimmer Biomet Affixus Hip Fracture Nail Right 125 9 mm x 300 mm, Item Number 814309300 recall — FDA Z-0124-2019

There were complaints indicating that when the product was opened in surgery, the sterile packaging was already open.

Class IIFDA: TerminatedZimmer Biomet, Inc.

Medical DeviceOct 24, 2018

Zimmer Biomet Affixus Hip Fracture Nail Right 130 11 mm x 360 mm, Item Number 814511360 recall — FDA Z-0161-2019

There were complaints indicating that when the product was opened in surgery, the sterile packaging was already open.

Class IIFDA: TerminatedZimmer Biomet, Inc.

Medical DeviceOct 24, 2018

Helena Laboratories "Free and Total Protein S ELISA Kit" Cat recall — FDA Z-0106-2019

Internal components of the Protein S ELISA Antigen Kit (Lot: 3-16-5292) were mislabeled. The Protein S Conjugate Solution is labeled as Substrate, and the Substrate is labeled as Protein S…

Class IIFDA: TerminatedHelena Laboratories, Inc.

Medical DeviceOct 24, 2018

Siemens Medical Solutions USA Biograph Horizon a) 3R, Material Number 10532746 b) 4R recall — FDA Z-0177-2019

The terminals on the plug may become loose and overheat.

Class IIFDA: TerminatedSiemens Medical Solutions USA, Inc.

Medical DeviceOct 24, 2018

Zimmer Biomet Affixus Hip Fracture Nail Left 125 9 mm x 260 mm, Item Number 814409260 recall — FDA Z-0145-2019

There were complaints indicating that when the product was opened in surgery, the sterile packaging was already open.

Class IIFDA: TerminatedZimmer Biomet, Inc.

Medical DeviceOct 24, 2018

Zimmer Biomet Affixus Hip Fracture Nail Right 125 9 mm x 440 mm, Item Number 814309440 recall — FDA Z-0129-2019

There were complaints indicating that when the product was opened in surgery, the sterile packaging was already open.

Class IIFDA: TerminatedZimmer Biomet, Inc.

Medical DeviceOct 24, 2018

Philips HeartStart FR3 Defibrillator, Model: 861388, 861389 Product Usage: The HeartStart recall — FDA Z-0175-2019

Automated external defibrillators may not fully meet IPx5 water ingress specification. The device may fail to function should water intrusion occur.

Class IIFDA: TerminatedPhilips Electronics North America Corp.

Medical DeviceOct 24, 2018

Zimmer Biomet Affixus Hip Fracture Nail Right 125 11 mm x 420 mm, Item Number 814311420 recall — FDA Z-0135-2019

There were complaints indicating that when the product was opened in surgery, the sterile packaging was already open.

Class IIFDA: TerminatedZimmer Biomet, Inc.

Medical DeviceOct 24, 2018

Zimmer Biomet Affixus Hip Fracture Nail Left 130 15 mm x 360 mm, Item Number 814615360 recall — FDA Z-0168-2019

There were complaints indicating that when the product was opened in surgery, the sterile packaging was already open.

Class IIFDA: TerminatedZimmer Biomet, Inc.

Medical DeviceOct 24, 2018

Zimmer Biomet Affixus Hip Fracture Nail Left 125 9 mm x 300 mm, Item Number 814409300 recall — FDA Z-0146-2019

There were complaints indicating that when the product was opened in surgery, the sterile packaging was already open.

Class IIFDA: TerminatedZimmer Biomet, Inc.

Medical DeviceOct 24, 2018

Zimmer Biomet Affixus Hip Fracture Nail Right 125 9 mm x 340 mm, Item Number 814309340 recall — FDA Z-0126-2019

There were complaints indicating that when the product was opened in surgery, the sterile packaging was already open.

Class IIFDA: TerminatedZimmer Biomet, Inc.

Medical DeviceOct 24, 2018

Zimmer Biomet Affixus Hip Fracture Nail Left 125 11 mm x 260 mm, Item Number 814411260 recall — FDA Z-0150-2019

There were complaints indicating that when the product was opened in surgery, the sterile packaging was already open.

Class IIFDA: TerminatedZimmer Biomet, Inc.

Medical DeviceOct 24, 2018

Zimmer Biomet Affixus Hip Fracture Nail Right 125 13 mm x 260 mm, Item Number 814313260 recall — FDA Z-0139-2019

There were complaints indicating that when the product was opened in surgery, the sterile packaging was already open.

Class IIFDA: TerminatedZimmer Biomet, Inc.

Medical DeviceOct 24, 2018

Zimmer Biomet Affixus Hip Fracture Nail - Left 125 11mm x 340mm, Item Number 814411340 recall — FDA Z-0152-2019

There were complaints indicating that when the product was opened in surgery, the sterile packaging was already open.

Class IIFDA: TerminatedZimmer Biomet, Inc.

Medical DeviceOct 24, 2018

Siemens Healthcare Diagnostics ADVIA Centaur CKMB Master Curve Material, Cat No. 07867768 recall — FDA Z-0115-2019

A potential bias was identified with certain kits compared to the internal standards.

Class IIFDA: TerminatedSiemens Healthcare Diagnostics, Inc.

Medical DeviceOct 24, 2018

OriGen Biomedical Reinforced Dual Lumen Cannula, 19Fr., REF: VV19F, Sterile EO Indications recall — FDA Z-0181-2019

These catheters may have the following deficiencies: 1) barium sulfate omission, and 2) actual catheter tip length is one centimeter shorter than printed on the tip

Class IIFDA: TerminatedOriGen Biomedical, Inc.

Browse by month

Recent recall archives

Browse recent months with enough recall history for useful comparison.

Full archive →

October 2026243 records · 4 categories September 2026363 records · 4 categories August 2026302 records · 4 categories July 2026370 records · 4 categories June 2026376 records · 4 categories May 2026340 records · 4 categories April 2026415 records · 4 categories March 2026190 records · 4 categories February 2026331 records · 4 categories January 2026212 records · 4 categories December 2025389 records · 4 categories November 2025326 records · 4 categories