Latest U.S. Recalls — FDA & NHTSA Records

Latest records

Latest recalls — page 1746

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

DrugDec 21, 2016

Cantrell Drug Company Midazolam HCl 50 mg/50 mL in 0.9% Sodium Chloride (1 mg/mL) recall — FDA D-0198-2017

Lack of Assurance of Sterility - the firm is recalling select sterile drug products.

Class IIFDA: TerminatedCantrell Drug Company

DrugDec 21, 2016

Cantrell Drug Company Fentanyl Citrate 2 mcg/mL & Bupivacaine HCl 0.125% in 0.9% Sodium recall — FDA D-0190-2017

Lack of Assurance of Sterility - the firm is recalling select sterile drug products.

Class IIFDA: TerminatedCantrell Drug Company

DrugDec 21, 2016

Cantrell Drug Company Rocuronium Bromide 50 mg/5 mL Injection Solution, 5 mL (10 mg/mL) recall — FDA D-0202-2017

Lack of Assurance of Sterility - the firm is recalling select sterile drug products.

Class IIFDA: TerminatedCantrell Drug Company

DrugDec 21, 2016

Cantrell Drug Company Neostigmine Methylsulfate 5 mg/5 mL Injection Solution, 5 mL (1 mg/mL) recall — FDA D-0200-2017

Lack of Assurance of Sterility - the firm is recalling select sterile drug products.

Class IIFDA: TerminatedCantrell Drug Company

DrugDec 21, 2016

Cantrell Drug Company Glycopyrrolate 1 mg/5 mL (0.2 mg/mL) Injection Solution, 5 mL recall — FDA D-0191-2017

Lack of Assurance of Sterility - the firm is recalling select sterile drug products.

Class IIFDA: TerminatedCantrell Drug Company

DrugDec 21, 2016

Cantrell Drug Company Heparin Sodium 5,000 USP Units Added to 0.9% Sodium Chloride 1,000 mL* recall — FDA D-0193-2017

Lack of Assurance of Sterility - the firm is recalling select sterile drug products.

Class IIFDA: TerminatedCantrell Drug Company

DrugDec 21, 2016

Cantrell Drug Company Calcium Chloride (20 mg/mL) in 0.9% Sodium Chloride 500 mL Bag recall — FDA D-0186-2017

Lack of Assurance of Sterility - the firm is recalling select sterile drug products.

Class IIFDA: TerminatedCantrell Drug Company

DrugDec 21, 2016

Cantrell Drug Company Succinylcholine Chloride 200 mg/10 mL Injection Solution 10 mL recall — FDA D-0204-2017

Lack of Assurance of Sterility - the firm is recalling select sterile drug products.

Class IIFDA: TerminatedCantrell Drug Company

DrugDec 21, 2016

Cantrell Drug Company Ropivacaine HCl 0.25% in 0.9% Sodium Chloride, 100 mL Bag, Epidural recall — FDA D-0203-2017

Lack of Assurance of Sterility - the firm is recalling select sterile drug products.

Class IIFDA: TerminatedCantrell Drug Company

DrugDec 21, 2016

Cantrell Drug Company HYDROmorphone HCl 6 mg/30 mL in 0.9% Sodium Chloride (0.2 mg/mL) recall — FDA D-0194-2017

Lack of Assurance of Sterility - the firm is recalling select sterile drug products.

Class IIFDA: TerminatedCantrell Drug Company

DrugDec 21, 2016

Cantrell Drug Company Fentanyl Citrate 1,500 mcg in 0.9% Sodium Chloride (10 mcg/mL) 150 mL recall — FDA D-0188-2017

Lack of Assurance of Sterility - the firm is recalling select sterile drug products.

Class IIFDA: TerminatedCantrell Drug Company

DrugDec 21, 2016

Jubilant Cadista Pharmaceuticals Methylprednisolone Tablets, USP, 16 mg, 50-count bottles recall — FDA D-0205-2017

Labeling: Incorrect or Missing Lot and/or Exp Date: incorrect expiration date of 02/0218 is printed on the container label instead of the correct expiration date of 02/2018.

Class IIIFDA: TerminatedJubilant Cadista Pharmaceuticals, Inc.

DrugDec 21, 2016

Cantrell Drug Company Heparin Sodium, 1 USP Unit/2 mL (0.5 USP Units/mL) in 0.45% Sodium recall — FDA D-0192-2017

Lack of Assurance of Sterility - the firm is recalling select sterile drug products.

Class IIFDA: TerminatedCantrell Drug Company

DrugDec 21, 2016

Cantrell Drug Company Fentanyl Citrate 2,500 mcg in 0.9% Sodium Chloride (10 mcg/mL) 250 mL* recall — FDA D-0189-2017

Lack of Assurance of Sterility - the firm is recalling select sterile drug products.

Class IIFDA: TerminatedCantrell Drug Company

DrugDec 21, 2016

Cantrell Drug Company HYDROmorphone HCl 50 mg/50 mL in 0.9% Sodium Chloride (1 mg/mL) recall — FDA D-0195-2017

Lack of Assurance of Sterility - the firm is recalling select sterile drug products.

Class IIFDA: TerminatedCantrell Drug Company

DrugDec 21, 2016

Cantrell Drug Company Oxytocin 30 USP Units Added to 0.9% Sodium Chloride, 500 mL Bag recall — FDA D-0201-2017

Lack of Assurance of Sterility - the firm is recalling select sterile drug products.

Class IIFDA: TerminatedCantrell Drug Company

Medical DeviceDec 14, 2016

Merge Healthcare Merge, eFilm Workstation and eFilm Lite eFilm Workstation with Modules is a recall — FDA Z-0707-2017

A product issues happens for RF projection images. If user measures on RF image, .cal (Calibration) is not displayed and measurement is not correct. The .cal label is not displayed on the…

Class IIFDA: TerminatedMerge Healthcare, Inc.

Medical DeviceDec 14, 2016

Angiodynamics Peripherally Inserted Central Catheters (PICC), UPN H965750191, Catalog # recall — FDA Z-0715-2017

There is a potential for stylet stiffening that is not accurately represented on the labeling. The label states that product includes a stylet with an outside diameter (OD) measuring 0.014,…

Class IIFDA: TerminatedAngiodynamics Inc. (Navilyst Medical Inc.)

Medical DeviceDec 14, 2016

Ivoclar Vivadent Virtual XD Refill Light Body Fast Set Wash Material, 2X50 ml, REF #/Product recall — FDA Z-0717-2017

The firm received complaints claiming the dental material failed to set up. As the dental material ages, the set time may increase.

Class IIFDA: TerminatedIvoclar Vivadent, Inc.

Medical DeviceDec 14, 2016

Philips Medical Systems (Cleveland) Brilliance 64 728232 Computed Tomography X-ray systems recall — FDA Z-0694-2017

Software error due to the filament on timer

Class IIFDA: TerminatedPhilips Medical Systems (Cleveland) Inc.

Medical DeviceDec 14, 2016

3M Company - Health Care Business 3M Universal Electrosurgical Pad, REF 9130 recall — FDA Z-0701-2017

3M is recalling Universal Electrosurgical Pads because a report of an unintended material (process liner) in the product. This may prevent or impede the safe return of electrosurgical…

Class IIFDA: Terminated3M Company - Health Care Business

Medical DeviceDec 14, 2016

Medtronic Neuromodulation Model 37751 Recharger Product Usage: The Medtronic 37751 Recharger recall — FDA Z-0700-2017

Medtronic has identified an increased number of complaints from customers involving reports of Rechargers (Medtronic Model 37751 Recharger, which is included in Models 37754 and 97754…

Class IIFDA: TerminatedMedtronic Neuromodulation

Medical DeviceDec 14, 2016

Ivoclar Vivadent Virtual XD Refill Light Body Regular Set Wash Material, 2X50 ml, REF recall — FDA Z-0718-2017

The firm received complaints claiming the dental material failed to set up. As the dental material ages, the set time may increase.

Class IIFDA: TerminatedIvoclar Vivadent, Inc.

Medical DeviceDec 14, 2016

Philips Medical Systems (Cleveland) IQon Spectral CT is a Computed Tomography X-Ray System recall — FDA Z-0705-2017

A software defect is causing issues with the IQon Spectral CT and Philips Spectral CT Applications while filming, saving and annotating images

Class IIFDA: TerminatedPhilips Medical Systems (Cleveland) Inc.

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