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Cardinal Health Presource Kits recallZ-0912-2025 · Cardinal Health 200, LLC · initiated Nov 8, 2024

Open, Classified

Is my device affected?

  1. Compare the model, catalog and lot or serial numbers on your device or its packaging with the code information below. A recall usually covers only specific models or lots.
  2. If yours is listed, follow the instructions from Cardinal Health 200, LLC or your healthcare provider. The company's action is summarized under what the company is doing.
  3. Do not stop using a prescribed or implanted device on your own — talk to your healthcare provider first.

Where to find your model and lot numbers · What recall classes and statuses mean

Why it was recalled

Potential endotoxin contamination in non-sterile surgical strips and patties in Presource kits.

FDA root cause category: Nonconforming Material/Component

What the company is doing

An URGENT: PRODUCT RECALL notification letter dated 11/8/24 was sent to customers. If you locate affected product within your facility, please complete the following: 1. REVIEW your inventory immediately stop using the affected product code and lots attached. 2. COMMUNICATE with all personnel who utilize the Presource Kits containing CODMAN Patties & Strips component produced by Integra LifeSciences. 3. NOTIFY any customers to whom you may have distributed/forwarded affected product or to whom you plan to send the product about this medical device product correction and share a copy of this notice. 1. RETURN the enclosed acknowledgment form via fax to 614-652-9648 or email to [email protected], whether you have affected product or not. For Presource kit credit or replacement, please contact the following: " Hospitals Cardinal Customer Service at 866.551.0533 " Distributors Distributor Management at 800.635.6021 " Federal Government facilities Government Customer Service at 800.444.1166 If you are a Distributor and have further distributed affected kits, please notify your customers of this recall. In the event you have experienced quality problems or adverse events related to the products listed above, please utilize the contacts above to report the event. Should you have any questions, require additional labels or desire special assistance relating to this recall, please feel free to contact Cardinal Health Quality Systems at 800.292.9332.

Recall details

Recall number
Z-0912-2025
Status
Open, Classified
Initiated by the company
Nov 8, 2024
Posted by the FDA
Jan 15, 2025
Recalling firm
Cardinal Health 200, LLC
Quantity
512,786 total units
Product code
OGH
Distribution
Worldwide distribution - US Nationwide and the countries of Canada, Saudi Arabia.

Product description

Cardinal Health Presource Kits: 1 ) LARYNGOSCOPY PACK, Catalog Number: SEN11LGUH2 ; 2 ) LARYNGOSCOPY PACK, Catalog Number: SEN11LGUH3 ; 3 ) LARYNGOSCOPY PACK, Catalog Number: SEN11LGUH4 ; 4 ) LARYNGOSCOPY PACK, Catalog Number: SEN11LGUH5 ; 5 ) STERILE LARYNGOSCOPY PACK, Catalog Number: SEN11LGUHB

Code information (models, lots, serial numbers)

Show the full code information (2k characters)

Catalog Number SEN11LGUH2, UDI/DI 10195594093310 (EA)50195594093318 (CS), Lot Number J86T83 ; Catalog Number SEN11LGUH3, UDI/DI 10195594169626 (EA)50195594169624 (CS), Lot Number 5140349 ; Catalog Number SEN11LGUH4, UDI/DI 10195594230333 (EA)50195594230331 (CS), Lot Number 5405627 ; Catalog Number SEN11LGUH5, UDI/DI 10195594321871 (EA)50195594321879 (CS), Lot Number J6278U ; Catalog Number SEN11LGUHB, UDI/DI 10887488360911 (EA)50887488360919 (CS), Lot Number J43U76 ; Catalog Number SEN11LGUHB, UDI/DI 10887488360911 (EA)50887488360919 (CS), Lot Number J5679F ; Catalog Number SEN11LGUHB, UDI/DI 10887488360911 (EA)50887488360919 (CS), Lot Number J5679F ; Catalog Number SEN11LGUHB, UDI/DI 10887488360911 (EA)50887488360919 (CS), Lot Number J5679G ; Catalog Number SEN11LGUHB, UDI/DI 10887488360911 (EA)50887488360919 (CS), Lot Number J74A30 ; Catalog Number SEN11LGUHB, UDI/DI 10887488360911 (EA)50887488360919 (CS), Lot Number J8064Z ; Catalog Number SEN11LGUHB, UDI/DI 10887488360911 (EA)50887488360919 (CS), Lot Number J8123W ; Catalog Number SEN11LGUHB, UDI/DI 10887488360911 (EA)50887488360919 (CS), Lot Number J8393U ; Catalog Number SEN11LGUHB, UDI/DI 10887488360911 (EA)50887488360919 (CS), Lot Number J8692W ; Catalog Number SEN11LGUHB, UDI/DI 10887488360911 (EA)50887488360919 (CS), Lot Number J8671P ; Catalog Number SEN11LGUHB, UDI/DI 10887488360911 (EA)50887488360919 (CS), Lot Number J86T83 ; Catalog Number SEN11LGUHB, UDI/DI 10887488360911 (EA)50887488360919 (CS), Lot Number 5664098 ; Catalog Number SEN11LGUHB, UDI/DI 10887488360911 (EA)50887488360919 (CS), Lot Number 5631073 ;

Devices named in this recall

5 devices in the FDA device registry whose identifier appears in the recall's code information.

Other products in the same recall event

The FDA groups related products into one recall event (event 95722).

Sources and updates

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