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The Metrix Company

The Metrix Company Recalls

All product recalls associated with The Metrix Company.

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Recall Summary

Total Recalls

1000

Past Year

1000

Class I (Serious)

145

Most Recent

Jan 2026

Data from FDA, USDA, CPSC, and NHTSA public records. Recall counts vary by company size, industry, and reporting practices. Always check official sources for current information.

Showing 2701–2720 of 37661 recalls

Vygon 250mL EVA Container (Metrix) – IV Bag Leak (2024)

A limited number of IV bags have been found to leak during filling.

FDAOct 9, 2024Nationwide• The Metrix Company

CORMIX 500 mL EVA Container (The Metrix Company) – IV Bag Leak Risk (2024)

A limited number of IV bags have been found to leak during filling.

FDAOct 9, 2024Nationwide• The Metrix Company

CORMIX 250 mL EVA Container (The Metrix Company) – IV Bag Leak Risk (2024)

A limited number of IV bags have been found to leak during filling.

FDAOct 9, 2024Nationwide• The Metrix Company

1...134 135136137 138...1884

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Cormix 150mL EVA Container (Metrix) – IV Bag Leak (2024)

A limited number of IV bags have been found to leak during filling.

Moderate

FDAOct 9, 2024Nationwide• The Metrix Company

SECURE 50 mL EVA Container (The Metrix Company) – IV Bag Leak Risk (2024)

A limited number of IV bags have been found to leak during filling.

FDAOct 9, 2024Nationwide• The Metrix Company

Cinacalcet Tablets 60mg (Dr. Reddy's) – Nitrosamine Impurity (2024)

CGMP Deviations: Presence of N-nitroso Cinacalcet impurity above FDA recommended interim limit

Class IIModerate

FDAOct 9, 2024Nationwide• Dr. Reddy's Laboratories, Inc.

Cinacalcet Tablets 90mg (Dr. Reddy's) – Nitrosamine Impurity (2024)

CGMP Deviations: Presence of N-nitroso Cinacalcet impurity above FDA recommended interim limit

Class IIModerate

FDAOct 9, 2024Nationwide• Dr. Reddy's Laboratories, Inc.

Cinacalcet Tablets 30mg (Dr. Reddy's) – Nitrosamine Impurity (2024)

CGMP Deviations: Presence of N-nitroso Cinacalcet impurity above FDA recommended interim limit

Class IIModerate

FDAOct 9, 2024Nationwide• Dr. Reddy's Laboratories, Inc.

Member's Mark Roasted Red Pepper Hummus (Cedar's) – Foreign objects (2024)

Potential presence of foreign objects.

Class IIModerate

FDAOct 9, 2024GA, IN, LA +7 more• Cedar's Mediterranean Foods, Inc.

MEDLINE Affected Kits (MEDLINE) – Smoke Evacuation Pencil Issue (2024)

Medline is recalling medical convenience manufactured using certain lots of SafeAir Smoke Evacuation Pencil which were subsequently recalled by Stryker.

FDAOct 9, 2024Nationwide• MEDLINE INDUSTRIES, LP Northfield

MONOCRYL Suture (ETHICON) – Component Mix-Up Risk (2024)

Due a component mix-up in manufacturing, the affected products may contain incorrect needle type/size and suture length.

FDAOct 8, 2024AL, AK, AZ +42 more• ETHICON, INC. Calle Durango 2751 Col. Parque Industrial Americas, Juarez Juarez Mexico

Approach Hydro ST Micro Wire Guide (Cook) – Incorrect Expiration Labels (2024)

Affected device lots have labels that state the incorrect expiration dates.

FDAOct 8, 2024Nationwide• Cook Incorporated

Pineapple and Apple Salad (Del Monte) – Undeclared walnuts (2024)

Undeclared Allergen

The product is being recalled due to an undeclared allergen - tree nuts (walnuts).

Class IIModerate

FDAOct 8, 2024IN, PA• Del Monte Fresh Produce N.A., Inc.

Approach CTO Micro Wire Guide (Cook) – Incorrect Expiration Labels (2024)

Affected device lots have labels that state the incorrect expiration dates.

FDAOct 8, 2024Nationwide• Cook Incorporated

DRG:HYBRiD-XL Insulin (DRG International) – Recalibration Failure (2024)

The user of the assay may either face a failure message during re-calibration of the Hybrid.XL instrument using the re-calibration R1 and R2 of the device or find controls out of specification (failed Control High) which causes a delay in results.

FDAOct 7, 2024Nationwide• DRG International, Inc.

Philips Zenition 70 (PHILIPS) – Mains Control Unit Fuse Issue (2024)

Potential for the Mains Control Unit board fuse may blow out during system start-up or during a procedure.

FDAOct 7, 2024Nationwide• PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. Veenpluis 4-6 Best Netherlands

Philips Zenition 50 (PHILIPS) – Mains Control Unit Fuse Issue (2024)

Potential for the Mains Control Unit board fuse may blow out during system start-up or during a procedure.

FDAOct 7, 2024Nationwide• PHILIPS MEDICAL SYSTEMS NEDERLAND B.V. Veenpluis 4-6 Best Netherlands

Stress-B-Plus Dietary Supplement (Nestle) – Potential Contamination (2024)

Nestle Health Science (NHS U.S., LLC) is initiating a recall of Douglas Labs Stress-B-Plus Dietary Supplement Tablets, 90 tablets per bottle. The bottle is white and made of plastic. Lot Numbers 50335944,50344396, expiration date 04/11/2026. The product is being recalled because of Incorrect formulation manufactured vs label claims. Product was manufactured with Niacin (as Nicotinic acid) and supplement facts panel states contains Niacin (as Niacinamide).

Class IIModerate

FDAOct 7, 2024AK, AZ, CA +32 more• Nestle Product Technology Center - Nestle Health Science

CardioMEMS HF System (St. Jude Medical) – Cloud Data Migration Error (2024)

As a result of a cloud data migration of Patient and Hospital Electronic Systems (PES and HES) reverted to an outdated configuration causing incorrect/inaccurate pulmonary artery (PA) pressure readings.

FDAOct 5, 2024Nationwide• St. Jude Medical

Arthroscopy Kit (MEDLINE) – Packaging Seal Defect (2024)

Products within a Medline pack may be impacted by a packaging error in which an incomplete seal has formed on the packaging thereby creating a packaging seal gap.

FDAOct 4, 2024Nationwide• MEDLINE INDUSTRIES, LP Northfield