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Abbott Diagnostic International, Ltd. 30 Bo Cruce Davila

Abbott Diagnostic International, Ltd. 30 Bo Cruce Davila Recalls

All product recalls associated with Abbott Diagnostic International, Ltd. 30 Bo Cruce Davila.

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Recall Summary

Total Recalls

1000

Past Year

144

Class I (Serious)

154

Most Recent

Dec 2025

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 1201–1220 of 1339 recalls

Abbott Diagnostic International, Ltd. 30 Bo Cruce Davila: TDx/TDxFLx Methotrexate II Reagent-List Number 07A12-60 -...

Incorrect configuration: kits contain reagent bottles in the order S-W-T-P instead of the correct order, W-S-T-P.

FDAMar 20, 2007AR, CA, CO +33 more• Abbott Diagnostic International, Ltd. 30 Bo Cruce Davila

Scanlan International Inc: SCANLAN International Mobin-Uddin Vein Holder, Sterile, D...

Incorrectly assembled by manufacturer

FDAFeb 19, 2007IN, MO• Scanlan International Inc

International Technidyne Corp.: International Technidyne Corporation (ITC) ProTime Microc...

Incorrect Test Results-ProTime ITC''s Microcoagulation System: Professional Instrument may report incorrect test results when more than 50 tests are in the memory and the technician uses the AUTO Send or PRINT RESULTS feature.

FDA

1...59 606162 63...67

Page 61 of 67Next

Dec 6, 2006

Nationwide

• International Technidyne Corp.

ARC Bicycle Light Batteries (Light & Motion) – Fire Risk (2006)

Fire/Burn Risk

The recalled batteries are found in Light & Motion 2004 ARC Li-Ion HID lighting systems. The lights are black with "ARC" and "LIGHT & MOTION" written in yellow letters. The recall includes only batteries with a manufacturer date code of 1003 or 1103. The date code is stamped on the bottom of the battery and "LIGHT & MOTION" is printed on the side of the battery.

CPSCOct 17, 2006Nationwide• GP Batteries International Ltd., of Singapore

Arrow International Inc: Implantable Vascular Access System -- Infusion Ports with...

Catheter has separated from the infusion port body.

FDASep 29, 2006Nationwide• Arrow International Inc

Abbott Diagnostic International, Ltd. Carr 2 Km 58.0 Cruce Davila: Abbott AxSYM Matrix Cells--Product List No: 8A73-02, sold...

Increase in complaints regarding controls out of range, calibration errors, and discrepant patient results with the AxSYM Troponin-I ADV assay.

FDASep 8, 2006Nationwide• Abbott Diagnostic International, Ltd. Carr 2 Km 58.0 Cruce Davila

Abbott Diagnostic International, Ltd. Carr 2 Km 58.0 Cruce Davila: Abbott AxSYM system FSH Master Calibrators (LN 7A60-30),...

Following a customer complaint, Abbott found an atypical stability profile for the lot of the calibrators listed in this recall. The investigation to date has shown that both controls and patient results have shifted upwards over time together.

FDASep 7, 2006PR• Abbott Diagnostic International, Ltd. Carr 2 Km 58.0 Cruce Davila

Abbott Diagnostic International, Ltd. Carr 2 Km 58.0 Cruce Davila: Architect FSH Calibrators (LN 6C24-01), for in vitro diag...

FDASep 7, 2006PR• Abbott Diagnostic International, Ltd. Carr 2 Km 58.0 Cruce Davila

Abbott Diagnostic International, Ltd. Carr 2 Km 58.0 Cruce Davila: FSH Calibrators (LN 9C06-01), for in vitro diagnostic use.

FDASep 7, 2006PR• Abbott Diagnostic International, Ltd. Carr 2 Km 58.0 Cruce Davila

Garden Treasures Fireplace (Agio) – fire hazard (2006)

Fire/Burn Risk

The recalled fireplace consists of a round fire bowl that rests on four legs, with a chimney cap and hood. The fireplace is made of steel and is painted black. They are about 3 feet tall and 2 feet wide. The item number, 91023, is printed on the package materials.

CPSCAug 29, 2006Nationwide• Agio International Company, Limited, of Hong Kong

Lawnmower Blades (Blount) – replacement defect (2006)

Laceration Risk

The recalled replacement lawnmower blades are intended for use on Snapper riding lawnmowers. The recalled blades are sold for use as replacement parts under the Oregon® and Silver Streak® brands only. Original equipment blades on Snapper lawnmowers and "Snapper" brand replacement blades are not included in this recall. The recalled blades are red and marked "MADE IN USA," "GRASS SIDE CX", "Oregon" or "SILVER STREAK." The part number and date code are engraved on one side of the blade. The recalled blades are part numbers: 99-111, 99-112, 99-113, 99-114, 99-117, 99-118, 99-926, 99-930 and date codes: BL, BM, BN, BP, BQ, BR, BS, BT, BU, BV, BW, BX, BY, BZ, CA, CB, CC, CD, CE, CF, CG, CH, CJ, CK, CL, CM, CN, CP.

CPSCAug 23, 2006Nationwide• Blount International Inc., of Kansas City, Mo.

Cage Bell Musical Instrument (Kindermusik) – choking risk (2006)

Choking Hazard

The musical instrument is a wooden cylinder with end caps and wooden dowels connecting the caps. A single bell is in the middle. Model number 5-30-00740 is sold individually; Model number 0-06-09005 is sold as part of a kit called Busy Days Home, which also contains a board book, a compact disc and a poster. The model number is written on the outside packaging of the product.

CPSCAug 17, 2006Nationwide• Kindermusik International Inc., of Greensboro, N.C.

International Medsurg Connection, Inc.: Allegiance Esmark 6' x 108' Bandage, Latex Free, Sterile;...

The bandages labeled as sterile had not been sterilized prior to distribution.

FDAAug 16, 2006Nationwide• International Medsurg Connection, Inc.

International Medsurg Connection, Inc.: Allegiance Esmark 4' x 144' Bandage, Latex Free, Sterile;...

The bandages labeled as sterile had not been sterilized prior to distribution.

FDAAug 16, 2006Nationwide• International Medsurg Connection, Inc.

International Medsurg Connection, Inc.: Allegiance Esmark 6' x 144' Bandage, Latex Free, Sterile;...

The bandages labeled as sterile had not been sterilized prior to distribution.

FDAAug 16, 2006Nationwide• International Medsurg Connection, Inc.

International Medsurg Connection, Inc.: Allegiance Esmark 4' x 108' Bandage, Latex Free, Sterile;...

The bandages labeled as sterile had not been sterilized prior to distribution.

FDAAug 16, 2006Nationwide• International Medsurg Connection, Inc.

Reebok Children's Windsuit (Adjmi) – choking risk (2006)

Choking Hazard

The recalled Reebok children's windsuits are full-zip boys' polyester jacket and pants sets with a cotton lining and the name "Reebok" and/or Reebok's Vector logo embroidered on the chest of the jacket. The suits were sold in eight different color combinations: orange/navy, light blue/royal blue, red/navy, yellow/gunmetal, yellow/navy, blue/navy, green/navy and red/black.

CPSCJun 22, 2006Nationwide• Adjmi Apparel Group, of New York, N.Y. (Adjmi is an authorized licensee of children's apparel products of Reebok International Ltd., of Canton, Mass.)

Arrow International Inc: Arrow Double-Lumen Balloon Wedge Pressure Catheter, for s...

The print identifying the two extension lines, CVP Proximal and PA Distal, are reversed.

FDAJun 20, 2006IL, IN, MD +2 more• Arrow International Inc

Hebron International, Inc.: Soft Cosmetic Contact Lenses sold under the brand names: ...

Contact lenses were distributed and sold to inappropriate retail establishments without professional eye care involvement.

FDAMay 10, 2006Nationwide• Hebron International, Inc.

Emergency Smoke Hoods (EVAC) – Carbon Monoxide Risk (2006)

Fire/Burn Risk

These smoke hoods are one-time use respiratory devices that assist users with breathing, while escaping a fire. They include a transparent plastic hood that covers the user's head, and a canister that filters out toxic gases. "EVAC+™" or "EVAC-U8™" is printed on the canister.

CPSCApr 20, 2006Nationwide• Brookdale International Systems Inc., of Vancouver, British Columbia, Canada