Latest U.S. Recalls — FDA & NHTSA Records

Latest records

Latest recalls — page 1619

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

FoodJun 21, 2017

BrightFarms, Inc.: WDC Greenhouse Bright Farms Baby Kale 3 oz recall — FDA F-2361-2017

According to the firm, they have detected metal in their product. The firm learned of the problem through an internal verification techniques. The firm believes there is a risk of a health…

Class IIFDA: TerminatedBrightFarms, Inc.: WDC Greenhouse LLC

FoodJun 21, 2017

L.A. Lucky Import & Export L.A recall — FDA F-2376-2017

During follow-up investigation of imported Basil Seeds that were refused for the presence of Salmonella, it was discovered that 100 out of 300 cartons had been distributed.

Class IFDA: TerminatedL.A. Lucky Import & Export

FoodJun 21, 2017

General Mills Chocolate chip cookie dough larabars, 10 count , UPC recall — FDA F-2369-2017

Chocolate chip cookie dough larabars which contain cashews were incorrectly packaged in peanut butter cookie larabars boxes. The individual labeling on the chocolate chip cookie dough…

Class IIFDA: TerminatedGeneral Mills, Inc.

DrugJun 21, 2017

Pharmedium Services Potassium PHOSphate added to 0.9% Sodium Chloride, 20 mMol 100 mL Bag recall — FDA D-0912-2017

Labeling: Not Elsewhere Classified: Incorrect volume printed on the product label.

Class IIIFDA: TerminatedPharmedium Services, LLC

DrugJun 21, 2017

Pharmedium Services VANCOMYCIN HCl 1.5g in 300 mL 0.9% Sodium Chloride Injection USP recall — FDA D-0914-2017

Labeling: Not Elsewhere Classified: Incorrect volume printed on the product label.

Class IIFDA: TerminatedPharmedium Services, LLC

DrugJun 21, 2017

Pharmedium Services Potassium PHOSphate added to 0.9% Sodium Chloride, 15 mMol 100 mL Bag recall — FDA D-0910-2017

Labeling: Not Elsewhere Classified: Incorrect volume printed on the product label.

Class IIIFDA: TerminatedPharmedium Services, LLC

DrugJun 21, 2017

Pharmedium Services Potassium PHOSphate in 0.5% Dextrose, 7.5 mMol in 100 mL, Service Code recall — FDA D-0908-2017

Labeling: Not Elsewhere Classified: Incorrect volume printed on the product label.

Class IIFDA: TerminatedPharmedium Services, LLC

DrugJun 21, 2017

Pharmedium Services Potassium CHLORide added to 0.9% Sodium Chloride, 10mEq 100 mL Bag recall — FDA D-0907-2017

Labeling: Not Elsewhere Classified: Incorrect volume printed on the product label.

Class IIIFDA: TerminatedPharmedium Services, LLC

DrugJun 21, 2017

Pharmedium Services Potassium PHOSphate added to 0.9% Sodium Chloride, 10 mMol 100 mL Bag recall — FDA D-0911-2017

Labeling: Not Elsewhere Classified: Incorrect volume printed on the product label.

Class IIIFDA: TerminatedPharmedium Services, LLC

DrugJun 21, 2017

Pharmedium Services Potassium CHLORide added to 0.9% Sodium Chloride, 30mEq 100 mL Bag recall — FDA D-0906-2017

Labeling: Not Elsewhere Classified: Incorrect volume printed on the product label.

Class IIIFDA: TerminatedPharmedium Services, LLC

DrugJun 21, 2017

Bausch & Lomb NasalCrom (cromolyn sodium) Nasal Spray, USP, 5.2 mg per spray, 200 metered recall — FDA D-0899-2017

CGMP Deviations: Possibility of the presence of microbial contamination in the water used to manufacture this product lot.

Class IIFDA: TerminatedBausch & Lomb, Inc.

DrugJun 21, 2017

American Pharmaceutical Ingredients ESTRONE USP recall — FDA D-0919-2017

cGMP Deviations; lack of quality assurance.

Class IIFDA: TerminatedAmerican Pharmaceutical Ingredients LLC

DrugJun 21, 2017

Pharmedium Services VANCOMYCIN HCl 1.75g in 300 mL 0.9% Sodium Chloride Injection USP recall — FDA D-0915-2017

Labeling: Not Elsewhere Classified: Incorrect volume printed on the product label.

Class IIFDA: TerminatedPharmedium Services, LLC

DrugJun 21, 2017

Pharmedium Services Potassium PHOSphate added to 0.9% Sodium Chloride, 7.5 mMol 100 mL Bag recall — FDA D-0909-2017

Labeling: Not Elsewhere Classified: Incorrect volume printed on the product label.

Class IIIFDA: TerminatedPharmedium Services, LLC

DrugJun 21, 2017

Pharmedium Services VANCOMYCIN HCl 1.5g in 300 mL 5% Dextrose Injection USP, Service Code recall — FDA D-0916-2017

Labeling: Not Elsewhere Classified: Incorrect volume printed on the product label.

Class IIFDA: TerminatedPharmedium Services, LLC

DrugJun 21, 2017

Pharmedium Services Potassium PHOSphate added to 0.9% Sodium Chloride, 7 mMol 100 mL Bag recall — FDA D-0913-2017

Labeling: Not Elsewhere Classified: Incorrect volume printed on the product label.

Class IIIFDA: TerminatedPharmedium Services, LLC

Medical DeviceJun 14, 2017

Arrow International Pressure Injectable Two-Lumen Central Venous Catheterization Kit with recall — FDA Z-2273-2017

Arrow International initiated the recall due to reports of safety cover disengagement and needlestick injury for the BD Eclipse Needle that are packaged with certain Arrow products.

Class IIFDA: TerminatedArrow International Inc.

Medical DeviceJun 14, 2017

Roche Diagnostics Cobas connection module (CCM) - OUTPUT UNIT The module CCM enables a recall — FDA Z-2223-2017

a gap between the conveyor belt and the rack tray table (plastic part) may cause vibration of the 5 position racks during the transport. This issue can pose a potential risk to involved…

Class IIFDA: TerminatedRoche Diagnostics Corporation

Medical DeviceJun 14, 2017

Zimmer Biomet Spine Vitality Spinal Fixation System, Vitality T27 Final Drivers and Vitality recall — FDA Z-2318-2017

Zimmer Biomet is conducting a medical device recall for Vitality T27 Final Drivers and Vitality Torque Limiting Handle 90 in-lbs because when applying torque to tighten the closure top…

Class IIFDA: TerminatedZimmer Biomet Spine Inc.

Medical DeviceJun 14, 2017

ConvaTec Non-Rebreathing Mask, Reservoir Bag, Check Valve, Two Side Valves, with Tubing recall — FDA Z-2241-2017

Non-Rebreathing Mask, Reservoir Bag, Check Valve, Two Side Valves, with Tubing, Product Code 3230MM

Class IIFDA: TerminatedConvaTec, Inc.

Medical DeviceJun 14, 2017

Arrow International Radial Artery Catheterization Kit with Sharps Safety Features The Arrow recall — FDA Z-2296-2017

Arrow International initiated the recall due to reports of safety cover disengagement and needlestick injury for the BD Eclipse Needle that are packaged with certain Arrow products.

Class IIFDA: TerminatedArrow International Inc.

Medical DeviceJun 14, 2017

Baxter MiniCap Extended Life PD Transfer Set with Twist Clamp - Extra Short. 1 Unit recall — FDA Z-2246-2017

Connection issues between the PD transfer set catheter connector and an adapter may lead to leaks and contamination of the fluid pathway which may result in peritonitis.

Class IIFDA: TerminatedBaxter Healthcare Corporation

Medical DeviceJun 14, 2017

ConvaTec Oxygen Masks, Elongated (Under Chin), Adult High Conc., Non-Rebreather, 7ft O2 recall — FDA Z-2232-2017

Oxygen Masks, Elongated (Under Chin), Adult High Conc., Non-Rebreather, 7ft O2 Tubing, Check Valve, Two Side Valve, Product Code 108-E

Class IIFDA: TerminatedConvaTec, Inc.

Medical DeviceJun 14, 2017

ConvaTec Rebreather Oxygen Mask, Adult 7 (2.1 m) Tubing, Product Code 3104MM, Product Code recall — FDA Z-2236-2017

Rebreather Oxygen Mask, Adult 7 (2.1 m) Tubing, Product Code 3104MM, Product Code 9104-E, Product Code PMD06001

Class IIFDA: TerminatedConvaTec, Inc.

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