CLASS II ONGOING Device recall · Reported 20 Aug 2025 · FDA Enforcement Report

Robotic/Laparoscopy Kittner + Tail Large 4 Long X-Ray recalled

Carefree Surgical Specialties is recalling Carefree Surgical Specialties Robotic/Laparoscopy Kittner + Tail Large 4 Long X-Ray, distributed nationwide in the US. The recall was initiated on 1 Jul 2025 and the FDA has classified it as Class II.

Check your package

Lot, batch or date codesLot Code: Lot Number: 1595 UDI Code: Not Available
Quantity recalled20

Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.

Recall details

Recall number
Z-2281-2025
FDA event ID
97259
Recalling firm
Carefree Surgical Specialties, Nampa, ID
Classification
Class II
Status
Ongoing
Recall initiated
1 Jul 2025
FDA classified
8 Aug 2025
Reported
20 Aug 2025
Type
Voluntary: Firm initiated
Customers notified by
Letter
Reason category
Foreign Material

Timeline

1 Jul 2025Recall initiated by company
8 Aug 2025Classified by FDA+38 days
20 Aug 2025Published in enforcement report+12 days

Companies usually start a recall weeks before the FDA classifies and publishes it; the gap above is that lag.

Reason for recall

Due to two issues: 1. Product contamination (biological foreign matter) that could compromise sterility. 2. Incorrect quantity of gauze in sterile packaging

Foreign material recalls cover pieces of metal, plastic, glass, wood or other objects that got into the product during processing and could cause injury if eaten.

Product as listed by the FDA

Brand Name: Carefree Surgical Specialties Product Name: Robotic/Laparoscopy Kittner + Tail Large 4 Long X-Ray Detectable 5pk 25pk/CS Roll Gauzes Model/Catalog Number: 15508/25 Product Description: Robotic/Laparoscopy Kittner + Tail Large 4 Long X-Ray Detectable 5pk 25pk/CS Roll Gauzes

Where it was distributed

US Nationwide distribution in the states of KY, TX, FL, NC, CO, CA, ID, WV, NY, IL, IN, IA, MI, LA, WI, MT, VA, MA, TN, CT, AL, PA, MO, NJ, AR, OH, NE, AZ, MN, MD, GA, NC, WA, VT, OK, RI, SC, NH, VT, NV, OR.

Nationwide AlabamaArkansasArizonaCaliforniaColoradoConnecticutFloridaGeorgiaIowaIdahoIllinoisIndianaKentuckyLouisianaMassachusettsMarylandMichiganMinnesotaMissouriMontana

Questions about this recall

Is Robotic/Laparoscopy Kittner + Tail Large 4 Long X-Ray Detectable/CS Roll Gauzes recalled?

Yes. Carefree Surgical Specialties recalled Robotic/Laparoscopy Kittner + Tail Large 4 Long X-Ray Detectable/CS Roll Gauzes on 1 Jul 2025. The recall is Class II and its status is Ongoing. Recall number Z-2281-2025.

Why was it recalled?

Due to two issues: 1. Product contamination (biological foreign matter) that could compromise sterility. 2. Incorrect quantity of gauze in sterile packaging

Which lots are affected?

Lot Code: Lot Number: 1595 UDI Code: Not Available

Where was it sold?

US Nationwide distribution in the states of KY, TX, FL, NC, CO, CA, ID, WV, NY, IL, IN, IA, MI, LA, WI, MT, VA, MA, TN, CT, AL, PA, MO, NJ, AR, OH, NE, AZ, MN, MD, GA, NC, WA, VT, OK, RI, SC, NH, VT, NV, OR.

What should I do if I have it?

Stop using the device if the notice says to, and contact the manufacturer or your healthcare provider for the correction or replacement.

What does Class II mean?

Class II means the product may cause temporary or medically reversible health problems, or the probability of serious harm is remote.

Read the official FDA notice · Source record retrieved 21 Sep 2026. The FDA describes openFDA data as unvalidated; the official notice takes precedence. This page reports the record and gives no medical advice.

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