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Omrix Biopharmaceuticals, Ltd. Plasma Fract. Inst. Magen David Adom Blood Services Ctr., Sheba Hospital Ramat Gan Israel

Omrix Biopharmaceuticals, Ltd. Plasma Fract. Inst. Magen David Adom Blood Services Ctr., Sheba Hospital Ramat Gan Israel Recalls

All product recalls associated with Omrix Biopharmaceuticals, Ltd. Plasma Fract. Inst. Magen David Adom Blood Services Ctr., Sheba Hospital Ramat Gan Israel.

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Recall Summary

Total Recalls

1000

Past Year

295

Class I (Serious)

116

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 4241–4260 of 4465 recalls

Omrix Biopharmaceuticals, Ltd. Plasma Fract. Inst. Magen David Adom Blood Services Ctr., Sheba Hospital Ramat Gan Israel: Crosseal, fibrin sealant (human), This package***, One Ap...

5 mL Crosseal fibrin sealant (human) is difficult to expel from the device resulting in product leakage from the vial insertion port .

FDAAug 6, 2004Nationwide• Omrix Biopharmaceuticals, Ltd. Plasma Fract. Inst. Magen David Adom Blood Services Ctr., Sheba Hospital Ramat Gan Israel

Medibo N.V. Heikant 5 Hanmont, Achel Belgium: Minerva Patient Lift, model ML-20; this lift has a passiv...

The hanger bar may detach from the jib yoke, the M8 bolt in the foot pedal assembly may come loose, and some units may have faulty actuator brackets on the mast assembly, resulting in the patient lift becoming unstable and allowing the patient to fall.

FDAAug 4, 2004CA, FL, LA +7 more• Medibo N.V. Heikant 5 Hanmont, Achel Belgium

Abbott Laboratories Diagnostic Div: Abbott Clinical Chemistry AEROSET/ ARCHITECT c8000 Creati...

Precipitate formed in product.

1...211 212213214 215...224

Page 213 of 224Next

FDAJul 27, 2004Nationwide• Abbott Laboratories Diagnostic Div

Dade Behring Inc. Rte 896, Glasgow Business Community: BC Thrombin Reagent . Thrombin Time Test

The product does not demonstrate the expected prolonged thrombin times for specimens obtained from patients recieving heparin

FDAJul 21, 2004CT, FL, IL +5 more• Dade Behring Inc. Rte 896, Glasgow Business Community

Range Hoods (Bosch) – Blower Malfunction (2004)

The recalled range hoods were sold under the "Bosch" brand name and have model numbers DAH93xxUC and DAH94xxUC. The blowers have model numbers DHG4001UC and DHG6001UC. Date codes of the recalled units are 8309 through 8404. The date code appears as the first four digits of the FD number. The Bosch® brand, the model number and FD number can be found on the nameplates. The nameplate of the hood is located on the front side of the back wall of the air channel. The nameplate of the blower is located on at the left side of the housing. If the unit has a green dot by the nameplate, it has already been repaired. The Bosch® name also appears on the front of the hoods. The hoods have black, white or stainless steel finishes.

CPSCJul 20, 2004Nationwide• BSH Home Appliances Corp., of Huntington Beach, Calif.

Biosense Webster, Inc.: Stockert 70 Radio Frequency Ablation Generator

Generator Failure resulting increase of catheter temperature that could not be controlled by power reduction.

FDAJul 16, 2004Nationwide• Biosense Webster, Inc.

Abbott Health Products, Inc.: AxSYM Total B-hCG Reagent Pack

Complaints have been received for AxSYM Total B-hCG Reagents lots 17202Q100, 17556Q100 and 17387Q100 failing calibrations.

FDAJul 7, 2004Nationwide• Abbott Health Products, Inc.

B. Braun Medical, Inc.: Standard and Custom Spinal Trays with 5% Lidocaine Hydroc...

drug ampuls in kits contain particulates

FDAJul 6, 2004Nationwide• B. Braun Medical, Inc.

Cranbrook Bicycles (Huffy) – Potential Structural Failure (2004)

The recall involves single-speed "Cranbrook" bicycles with 26-inch wheels. The bicycles were sold in both men's (model 56462) and ladies' (model 56472) style frames. The name "Cranbrook" is printed on the frame of the bicycle. Serial numbers included in the recall range from SNHHE04C52556 to SNHHE04C64557. Serial numbers and model numbers are located on the bottom bracket of the frame, where the crank is attached to the bicycle.

CPSCJun 16, 2004Nationwide• Huffy Bicycle Company, of Springboro, Ohio

Abbott Laboratories HPD/ADD/GPRD: ABBOTT TestPack+Plus Strep A with On Board Controls (OBC)...

False Positive results may be obtained with the identified lots when using a negative patient sample or a negative control.

FDAJun 11, 2004IN• Abbott Laboratories HPD/ADD/GPRD

Abbott Laboratories, Inc: ARCHITECT c8000 Processing Module; List Number 01G06-01. ...

Process change in the manufacturing of the AC/DC driver board used on the analyzer may result in one or more of the solid state relays to fail during use.

FDAJun 10, 2004Nationwide• Abbott Laboratories, Inc

Kiddie Car Cruisers (Far East Brokers) – Ride-On Toy Safety Issue (2004)

The Kiddie Car Cruiser is a battery-operated ride-on toy car that measures about 27 inches high by 30 inches wide and 44 inches long. "Turbo" and "Cruiser" are printed on labels on the side of the ride-on toys.

CPSCJun 9, 2004Nationwide• Far East Brokers and Consultants Inc. (FEBC), of Jacksonville, Fla.

Dade Behring Inc. Rte 896, Glasgow Business Community: Berichrom Heparin Reagent (OWLD11). The reagent is a co...

Customers have reported a high rate of instrument error flags and calibration issues when using affected reagent.

FDAJun 7, 2004AZ, CA, CO +20 more• Dade Behring Inc. Rte 896, Glasgow Business Community

Bio-Rad Laboratories Inc: Bio-Rad brand ''TOX/See Drug Screen Test''; Catalog numb...

The device was producing false negative results for cocaine tests.

FDAJun 4, 2004IN• Bio-Rad Laboratories Inc

Abbott Health Products, Inc.: TDx/TDxFLx Opiates Reagent, Product list number: 9673-60

Abbott Diagnostics Division has found that the oxymorphone cross-reactivity information in the 'Specific Performance Characteristics' section of the TDx/TDxFLx Opiates Reagent package insert (commodity number 32-2087/R5) does not match the current product performance.

FDAMay 28, 2004Nationwide• Abbott Health Products, Inc.

Coast Mountain Spas (Coast Mountain® Spas, of Langley, British Columbia, Canada) – fire hazard (2004)

Fire/Burn Risk

The recalled Coast Mountain® spas have various model names, including Cypress, Seymour, Cowichan, Washington and Robson spas. The model name is located on the top corner of the spa. The recalled units have a capacitor made by Motors Capacitor Inc., which can be identified by a label on the motor that has the words, "Tiny Might." The spas have an acrylic liner with western red cedar siding and seat up to six adults.

CPSCMay 27, 2004Nationwide• Coast Mountain® Spas, of Langley, British Columbia, Canada

Biosense Webster, Inc.: Quickcable Autoclaveable Cable Electrode Cable

Mislabeling.

FDAMay 21, 2004Nationwide• Biosense Webster, Inc.

Boehringer Laboratories Inc: Boheringer Suction Regulator Model 7702L, Lot number 04D ...

The suction regulator incorporates a gauge for the verification of suction levels. The particular lot of gauges used in the production of the regulators exhibits a potential to develop a leak and cause the delivered suction to be inaccurate.

FDAMay 19, 2004AL, FL, MA +4 more• Boehringer Laboratories Inc

Boehringer Laboratories Inc: Boehringer Replacement Gauge Model 9071, Lot Number 200405.

FDAMay 19, 2004AL, FL, MA +4 more• Boehringer Laboratories Inc

Passport Stroller (Baby Trend) – Safety Defect (2004)

These Baby Trend strollers have the word "Passport" written on both sides of the canopy. Only "Passport" strollers with Model Number 1514, SKN number 190554 and manufacturing dates between July 10, 2003 and November 26, 2003 are being recalled. This information is printed on the lower frame of "Passport" strollers behind the seat.

CPSCMay 13, 2004Nationwide• Baby Trend, Inc., of Ontario, California