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Advanced Sterilization Products

Advanced Sterilization Products Recalls

All product recalls associated with Advanced Sterilization Products.

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Recall Summary

Total Recalls

1000

Past Year

1000

Class I (Serious)

143

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 31741–31760 of 37665 recalls

Sterrad CycleSure Biological Indicator (ASP) – color maintenance issue (2009)

Biological Indicator indicating a positive result does not maintain yellow color for the entire incubation period and some indicators experience media evaporation prior to the end of the labeled maximum incubation time.

FDAJun 23, 2009Nationwide• Advanced Sterilization Products

OEC Surgical Tracking System (GE) – headset placement error (2009)

GE Healthcare Surgery had discovered that using the Inverted Headset Placement is not a validated configuration with the IT 3000, 2500, 2500 plus, 3500, 3500 plus, ConneCTstat, and ConneCTstat Plus Surgical Navigation equipment.

FDAJun 22, 2009Nationwide• GE OEC Medical Systems, Inc

Celsite Access Port (B. Braun) – potential defect (2009)

B. Braun Interventional Systems was notified by B. Braun Medical France, the manufacturer of the Celsite Access port that they had received 11 reports of polyurethane (type P) catheter disconnections. B. Braun Medical France has decided to recall all Celsite ports supplied with the affected catheter lot. To date, B. Braun Interventional Systems (US) has not received any reports of catheter dis

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FDAJun 22, 2009Nationwide• B. Braun Interventional Systems

OEC Surgical Tracking System (GE) – headset placement error (2009)

Class IHigh

FDAJun 22, 2009Nationwide• GE OEC Medical Systems, Inc

Chiba Needle (Remington Medical) - Unsealed Pouches (2009)

Two unsealed pouches were identified after product release, compromising product sterility.

FDAJun 19, 2009CA, WI• Remington Medical Inc.

Battery Equalizers (SmartSpark) – Fire Risk (2009)

Fire/Burn Risk

The recalled battery equalizers are charge balancing devices designed to increase the performance and longevity of rechargeable batteries.

CPSCJun 18, 2009Nationwide• SmartSpark Energy Systems Inc., of Champaign, Ill.

V 40 Femoral Head (Stryker) - Sterilization Issue (2009)

Sterilization issue: During post-sterilization inspection of the outer blister packaging of the affected lots, it was determined that the outer blister did not meet the required minimum seal width.

FDAJun 18, 2009Nationwide• Stryker Howmedica Osteonics Corp.

Dall Miles Cable Grip System (Stryker) - Sterilization Issue (2009)

Sterilization issue: During post-sterilization inspection of the outer blister packaging of the affected lots, it was determined that the outer blister did not meet the required minimum seal width.

FDAJun 18, 2009Nationwide• Stryker Howmedica Osteonics Corp.

Pediatric Central Venous Catheter (Arrow) - Wire Guide Incompatibility (2009)

The spring wire guide is too large in diameter to pass through the needle, dilator and catheter.

FDAJun 17, 2009Nationwide• Arrow International Inc

PyroCarbon PIP Joint (Ascension) - Trial Size Mismatch (2009)

Trial product was larger than actual implant. Trial product was re-designed to more closely match the implant.

FDAJun 17, 2009Nationwide• Ascension Orthopedics, Inc

Heat Guns (Wagner Spray Tech) – fire risk (2009)

Fire/Burn Risk

The recalled heat guns emit hot air and are used for paint and flooring removal, defrosting freezers and water lines, bending plastic, hobbies, etc. Recalled models include the Milwaukee Heat Gun MHT3300, ACE HT3500 Heat Gun, and the Wagner Heat Gun HT3500 with date codes V300R through Z365R and A001R through A111R. The heat gun's name and model number are located on a black label on the bottom of the heat gun's barrel. The date code is stamped into the bottom of the handle near the power cord. The heat guns are black or yellow plastic and measure about 10 inches long, 8 inches high and 3 inches wide.

CPSCJun 17, 2009Nationwide• Wagner Spray Tech Corp., of Minneapolis, Minn.

Clipping Device (Boston Scientific) - Deployment Failure (2009)

The clip may not deploy or, if deployed, the clip may not release from the tissue.

FDAJun 17, 2009Nationwide• Boston Scientific Corporation

POWERSAIL Dilatation Catheter (Abbott) - Shaft Damage (2009)

Distal shaft of the POWERSAIL coronary Dilatation Catheters exhibits damage that may result in a leak of contrast material and functional failures.

FDAJun 17, 2009Nationwide• Abbott Vascular-Cardiac Therapies dba Guidant Corporation