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Yearly recall archive

U.S. Recalls in 2018

Complete FDA and NHTSA recall records dated in 2018, organized for browsing by month, category and recalling company.

5,460recall records

4categories

12months represented

Dec 26, 2018latest record date

Monthly breakdown

2018 recalls by month

Select a month to review the recall records reported during that period.

December 2018285 records · 4 categories November 2018342 records · 4 categories October 2018626 records · 4 categories September 2018393 records · 4 categories August 2018569 records · 4 categories July 2018356 records · 4 categories June 2018402 records · 4 categories May 2018613 records · 4 categories April 2018449 records · 3 categories March 2018523 records · 3 categories February 2018612 records · 3 categories January 2018290 records · 3 categories

2018 recalls — page 57

Records are ordered by the best available source date.

DrugSep 26, 2018

Beaumont Bio-med Skin Irritation & Itch Response Homeopathic Formula, 2 FL recall — FDA D-1192-2018

CGMP Deviations: products manufactured by contract manufacturer under conditions that could result in possible microbial contamination.

Class IIFDA: TerminatedBeaumont Bio-med, Inc.

VehicleSep 26, 2018

Volkswagen Jetta headlights recall — NHTSA campaign 18V671000

Volkswagen Group of America, Inc. (Volkswagen) is recalling certain 2019 Volkswagen Jetta vehicles equipped with LED headlights. The passenger side headlight may be incorrectly positioned,…

headlightsVolkswagen Group of America, Inc.

Medical DeviceSep 19, 2018

Intuitive Surgical da Vinci X/Xi EndoWrist 8mm Monopolar Curved Scissors Model No. 470179-14 recall — FDA Z-3025-2018

Monopolar Curved Scissor (MCS) instruments may be susceptible to developing cracks near the proximal edge of the extension tube. These cracks may fracture the plastic surrounding the…

Class IIFDA: OngoingIntuitive Surgical, Inc.

Medical DeviceSep 19, 2018

Zimmer Biomet Affixus Hip Fracture Nail Left 125 11 mm x 400 mm, Item Number: 814411400 recall — FDA Z-3094-2018

The set screw is not able to advance or reverse from the original position in the nail.

Class IIFDA: TerminatedZimmer Biomet, Inc.

Medical DeviceSep 19, 2018

Zimmer Biomet Affixus Hip Fracture Nail Left 125 9 mm x 320 mm, Item Number: 814409320 recall — FDA Z-3081-2018

The set screw is not able to advance or reverse from the original position in the nail.

Class IIFDA: TerminatedZimmer Biomet, Inc.

Medical DeviceSep 19, 2018

Zimmer Biomet Affixus Hip Fracture Nail Right 125 13 mm x 400 mm, Item Number: 814313400 recall — FDA Z-3074-2018

The set screw is not able to advance or reverse from the original position in the nail.

Class IIFDA: TerminatedZimmer Biomet, Inc.

Medical DeviceSep 19, 2018

Zimmer Biomet Affixus Hip Fracture Nail Left 125 9 mm x 420 mm, Item Number: 814409420 recall — FDA Z-3086-2018

The set screw is not able to advance or reverse from the original position in the nail.

Class IIFDA: TerminatedZimmer Biomet, Inc.

Medical DeviceSep 19, 2018

Zimmer Biomet Affixus Hip Fracture Nail Right 125 9 mm x 300 mm, Item Number 814309300 recall — FDA Z-3048-2018

The set screw is not able to advance or reverse from the original position in the nail.

Class IIFDA: TerminatedZimmer Biomet, Inc.

Medical DeviceSep 19, 2018

Zimmer Biomet Affixus Hip Fracture Nail Right 125 9 mm x 360 mm, Item Number: 814309360 recall — FDA Z-3050-2018

The set screw is not able to advance or reverse from the original position in the nail.

Class IIFDA: TerminatedZimmer Biomet, Inc.

Medical DeviceSep 19, 2018

Zimmer Biomet Affixus Hip Fracture Nail Right 130 9 mm x 300 mm, Item Number: 814509300 recall — FDA Z-3111-2018

The set screw is not able to advance or reverse from the original position in the nail.

Class IIFDA: TerminatedZimmer Biomet, Inc.

Medical DeviceSep 19, 2018

Zimmer Biomet Affixus Hip Fracture Nail Left 130 15 mm x 360 mm, Item Number: 814615360 recall — FDA Z-3174-2018

The set screw is not able to advance or reverse from the original position in the nail.

Class IIFDA: TerminatedZimmer Biomet, Inc.

Medical DeviceSep 19, 2018

Zimmer Biomet Affixus Hip Fracture Nail Left 125 11 mm x 340 mm, Item Number: 814411340 recall — FDA Z-3091-2018

The set screw is not able to advance or reverse from the original position in the nail.

Class IIFDA: TerminatedZimmer Biomet, Inc.

Medical DeviceSep 19, 2018

Zimmer Biomet Affixus Hip Fracture Nail Left 125 9 mm x 460 mm, Item Number: 814409460 recall — FDA Z-3088-2018

The set screw is not able to advance or reverse from the original position in the nail.

Class IIFDA: TerminatedZimmer Biomet, Inc.

Medical DeviceSep 19, 2018

SPS Sterilization Edwards Lifesciences Femoral Venous Cannula, 20F X 55CM, resterilized recall — FDA Z-3033-2018

The expiration date on the device labeling exceeds its actual validated shelf life because the sterilization process used does not have adequate support for the extended shelf life.

Class IIFDA: TerminatedSPS Sterilization, Inc.

Medical DeviceSep 19, 2018

Zimmer Biomet Affixus Hip Fracture Nail Left 130 11 mm x 260 mm, Item Number: 814611260 recall — FDA Z-3153-2018

The set screw is not able to advance or reverse from the original position in the nail.

Class IIFDA: TerminatedZimmer Biomet, Inc.

Medical DeviceSep 19, 2018

Zimmer Biomet Affixus Hip Fracture Nail Right 125 9 mm x 380 mm, Item Number: 814309380 recall — FDA Z-3051-2018

The set screw is not able to advance or reverse from the original position in the nail.

Class IIFDA: TerminatedZimmer Biomet, Inc.

Medical DeviceSep 19, 2018

Zimmer Biomet Affixus Hip Fracture Nail Right 130 11 mm x 360 mm, Item Number: 814511360 recall — FDA Z-3126-2018

The set screw is not able to advance or reverse from the original position in the nail.

Class IIFDA: TerminatedZimmer Biomet, Inc.

Medical DeviceSep 19, 2018

remel THIOGLYCOLLATE MEDIUM W/O IND recall — FDA Z-3017-2018

Products have intermittently failed performance testing during stability studies with various anaerobic microorganisms.

Class IIFDA: TerminatedRemel Inc.

Medical DeviceSep 19, 2018

Zimmer Biomet Affixus Hip Fracture Nail Right 130 11 mm x 340 mm, Item Number: 814511340 recall — FDA Z-3125-2018

The set screw is not able to advance or reverse from the original position in the nail.

Class IIFDA: TerminatedZimmer Biomet, Inc.

Medical DeviceSep 19, 2018

Zimmer Biomet Affixus Hip Fracture Nail Right 130 13 mm x 300 mm, Item Number: 814513300 recall — FDA Z-3135-2018

The set screw is not able to advance or reverse from the original position in the nail.

Class IIFDA: TerminatedZimmer Biomet, Inc.

Medical DeviceSep 19, 2018

Zimmer Biomet Affixus Hip Fracture Nail Right 130 15 mm x 440 mm, Item Number: 814515440 recall — FDA Z-3145-2018

The set screw is not able to advance or reverse from the original position in the nail.

Class IIFDA: TerminatedZimmer Biomet, Inc.

Medical DeviceSep 19, 2018

Zimmer Biomet Affixus Hip Fracture Nail Right 130 9 mm x 400 mm, Item Number: 814509400 recall — FDA Z-3116-2018

The set screw is not able to advance or reverse from the original position in the nail.

Class IIFDA: TerminatedZimmer Biomet, Inc.

Medical DeviceSep 19, 2018

Zimmer Biomet Affixus Hip Fracture Nail 130 9 mm x 180 mm, Item Number: 814509180 recall — FDA Z-3108-2018

The set screw is not able to advance or reverse from the original position in the nail.

Class IIFDA: TerminatedZimmer Biomet, Inc.

Medical DeviceSep 19, 2018

Zimmer Biomet Affixus Hip Fracture Nail Right 130 13 mm x 260 mm, Item Number: 814513260 recall — FDA Z-3133-2018

The set screw is not able to advance or reverse from the original position in the nail.

Class IIFDA: TerminatedZimmer Biomet, Inc.

About the 2018 recall archive

This archive groups records by their reported or recall date. It does not imply that every recall was initiated, announced and resolved during the same calendar year. Open the individual record for the exact dates and source details supplied by FDA or NHTSA.