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Atrium Medical Corporation

Atrium Medical Corporation Recalls

All product recalls associated with Atrium Medical Corporation.

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Recall Summary

Total Recalls

1000

Past Year

1000

Class I (Serious)

127

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 5261–5280 of 25000 recalls

Atrium Ocean Chest Drain (Atrium) – Temperature Excursion (2022)

Warehouse experienced temperature excursions in July and August 2021. It was determined that there were no associated harms to patients.

FDAOct 18, 2022Nationwide• Atrium Medical Corporation

Buprenorphine and Naloxone Sublingual Tablets (Sun Pharmaceutical) – Foreign Substance (2022)

Presence of Foreign Substance

Class IIModerate

FDAOct 18, 2022Nationwide• SUN PHARMACEUTICAL INDUSTRIES INC

VS3 Iridium Microscope (Visionsense) – Unspecified Issue (2022)

XXX

FDAOct 17, 2022Nationwide

1...262 263264265 266...1250

Page 264 of 1250Next

• Visionsense, Ltd. 20, Ha-Magshimim Petakh Tikva Israel

VS3 Iridium IR Microscope (Visionsense) – Optical Fiber Damage (2022)

Broken Optical fiber cable damage can occur through handling or bending and can lead to loss of functionality and heating/melting of the outer cable surface.

FDAOct 17, 2022Nationwide• Visionsense, Ltd. 20, Ha-Magshimim Petakh Tikva Israel

Chicken Salad Sandwich Tray (Albertsons) – undeclared cashews (2022)

Store printed label on products does not include Tree Nuts (Cashews) in the ingredient statement and the contains statement.

Class IHigh

FDAOct 17, 2022CO, NE, NM +2 more• Albertsons Companies LLC

ReadyMeals Chicken Salad Quad (Albertsons) – undeclared cashews (2022)

Store printed label on products does not include Tree Nuts (Cashews) in the ingredient statement and the contains statement.

Class IHigh

FDAOct 17, 2022CO, NE, NM +2 more• Albertsons Companies LLC

U-Line Outdoor Freezers – fire hazard (2022)

Fire/Burn Risk

This recall involves U-Line Outdoor Series 24-inch Built-In Convertible Freezers with model number U-1224FZRSOD-00A and manufactured between 2017-2018. They have serial number ranges between 1745627020001-1745627020009; 1746096040001-1746096040077; 1850469050001-1850469050003; and 1850469059001-1850469059003. The model number, serial number, and "U-Line" brand name are printed on a plate located in the top right interior of the unit.

CPSCOct 13, 2022Nationwide• U-Line Corporation, of Milwaukee, Wisconsin

Little Senses Shape Sorter (Addo Play) – choking risk (2022)

Choking Hazard

This recall involves the Early Learning Centre Little Senses Lights and Sounds Shape Sorter toys. The toy has a white and gray base, holds six colored, shaped pieces with lights, and makes sounds and music. "Little Senses" is printed on the side of the base. The toy was marketed for children between ages 6 to 36 months of age. The item code for the sorter toy 82756 is located on the base of the main unit. The batch code on the product is located on the base of the main unit, and corresponds to date of manufacture as follows: The two batch codes relate to the following production dates. Batch Code Production Date 1420WB01 May 21, 2020 3280WB01 Nov 23, 2020

CPSCOct 13, 2022Nationwide• Addo Play Ltd., of United Kingdom

Salted Caramel Cookies (Hammond's) – undeclared peanut (2022)

Undeclared Allergen

Peanut Butter Chocolate Chip Cookies mispacked in Salted Caramel Cookies Box creating undeclared peanut allergen.

Class IHigh

FDAOct 13, 2022Nationwide• Hammond's Candies Since 1920 II, LLC

BD Nexiva IV Catheter (Becton Dickinson) – Shield Separation Risk (2022)

During needle withdrawal, the tip shield may prematurely separate from the catheter adapter and preventing the needle tip from being in the safely shielded (leaving the needle tip exposed).

FDAOct 12, 2022FL, GA, IL +10 more• Becton Dickinson Infusion Therapy Systems Inc.

Basin Set (American Contract) – Labeling Mismatch (2022)

Basin Set labeling error: components within the kit are for the Single Basin Set. Therefore, the contents of the package do not match the contents listed on the label.

FDAOct 12, 2022Nationwide• American Contract Systems, Inc.

Alinity m System (Abbott) – Software Performance Issue (2022)

Abbott has identified potential performance issues for the Alinity m System software version 1.6.5: 1) In a unique scenario, the waste chute flapper was found to not open when the Systems Solution drawer was closed and locked. It was found that the software will cause the flapper door to stay in the closed position when the drawer is closed and locked if the flapper had previously been moved out of position. 2) Sample preparation drawer #1 barcode information is used instead of sample prep drawer #2 when the scanned data is not sent to the System Control Center before the next bottle barcode in sample prep drawer#2 is scanned. 3) Under a specific condition, while the system is processing tests and a new test request is made, when the level of the bulk solution is too low to process a test, the software would error stop the system and try to complete all in-process tests. An internal counter is reset which can cause reaction vessels (RVs) already present in an Amplification Detection Unit (or amp detect) to remain there and not be moved to waste so that more RVs can be placed into the amp detect for processing. 4) 4 to 6 replicates of the same auto calibrator orders can be run with 2 different sets of calibrator materials on the same rack. It was discovered during internal testing, when running 4 to 6 replicates of a calibrator, it is possible for the user to use 2 separate lots of material which is not detected by the System Control Center (SCC). If this were to occur, the calibration curve would be created using 2 separate material lots. In normal use scenario, this curve would be made using only 1 lot of material.

FDAOct 12, 2022Nationwide• Abbott Molecular, Inc.

Ram 4500 (Ram) – Brake Hose Diameter Problem (2022)

Chrysler (FCA US, LLC) is recalling certain 2019-2020 Ram 4500 and 5500 Cab Chassis vehicles. The rear brake hose inside diameter may be too small, which could cause the hose to rupture. As such, these vehicles fail to comply with the requirements of Federal Motor Vehicle Safety Standard number 106, "Brake Hoses."

NHTSAOct 11, 2022Nationwide• RAM

PAJUNK Epidural Tray (Pajunk) – Medication Labeling Error (2022)

The tray contains a 2ml ampule of 0.75% Marcaine Spinal in lieu of a 10ml ampule of 0.9% Sodium Chloride as intended,.

FDAOct 10, 2022Nationwide• Pajunk Medical Systems, L.P.