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Abbott Laboratories

Abbott Laboratories Recalls

All product recalls associated with Abbott Laboratories.

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Recall Summary

Total Recalls

1000

Past Year

1000

Class I (Serious)

145

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 35801–35820 of 37661 recalls

Abbott Laboratories: 18 French Ross Introducer Complete Gastrostomy Kit with B...

Gastrostomy and Jejunostomy primary placement kits which may contain components that may not have been adequately sterilized, were distributed.

FDANov 12, 2004Nationwide• Abbott Laboratories

Abbott Laboratories: 10 French Ross Flexiflo Lap J Laparoscopic Jejunostomy Ki...

Gastrostomy and Jejunostomy primary placement kits which may contain components that may not have been adequately sterilized, were distributed.

FDANov 12, 2004Nationwide• Abbott Laboratories

Abbott Laboratories: 20 French Ross Inverta-PEG Over-the-Guidewire Basic Gastr...

Gastrostomy and Jejunostomy primary placement kits which may contain components that may not have been adequately sterilized, were distributed.

FDA

1...1789 179017911792 1793...1884

Page 1791 of 1884Next

Nov 12, 2004

Nationwide

• Abbott Laboratories

Proctor & Gamble Co: The product is battery powered toothbrush. Spinbrush Pro ...

Market withdrawal of Crest Spinbrush Pro-Whitening. The firm has determined that there is a quality issue in certain production that may allow the circular brush at the tip of the brush head to become detached over time in a very small number of brushes.

FDANov 11, 2004Nationwide• Proctor & Gamble Co

Exactech, Inc.: Cemented Trapezoid Tibial Tray Sz. 4F/4T, Knee joint pate...

Implant was identified incorrectly at the time of manufacture and was then labeled and distributed with the incorrect size information.

FDANov 11, 2004FL, MD, MN +3 more• Exactech, Inc.

Smiths Medical MD, Inc.: Deltec branded PORT-A-CATH II Single-Lumen Low Profile Po...

The catheter became disconnected from the port while implanted in the patient.

FDANov 11, 2004FL, GA, IN +8 more• Smiths Medical MD, Inc.

The Straumann Company: Straumann Dental Implant System, SP Profile Drill, Short,...

Outside label incorrectly identifes drill as Regular Neck (RN) instead of Wide Neck (WN)

FDANov 11, 2004Nationwide• The Straumann Company

Proctor & Gamble Co: The product is refill heads for battery powered toothbrus...

FDANov 11, 2004Nationwide• Proctor & Gamble Co

Alaris Medical Systems Inc: Model 8100 Series Medley Medication Safety System Pump Mo...

The device modification is being implemented in response to information received from the field regarding a specific method of misloading the medication administration tubing set into the infusion system pump module. To date there have been complaints from three (3) different customer locations.

FDANov 10, 2004Nationwide• Alaris Medical Systems Inc

Soliras Headlamp Batteries (Black Diamond) – Battery Issue (2004)

Fire/Burn Risk

The recalled batteries are found in Black Diamond Soliras headlamps. The batteries have the following dates, which can be found on the battery label: 0703, 0803, 0903, 1003, 1103, 1203, 0104, 0204, 0304, 0404, and 0504. The black headlamp has the words and symbol for the company on the light.

CPSCNov 9, 2004Nationwide• Black Diamond Equipment Ltd., of Salt Lake City, Utah

Beckman Coulter Inc: Access Immunoassay Systems, 862.2160 discrete photometric...

A rare condition of the Access 2 Immunoassay Systems software versions 2.0, 2.1 and 2.2 could present a risk of an erroneous confirmatory result under a specific set of circumstances. The Chlamydia Blocking results may be affected. The instrument will erroneously perform the blocking calculation on the affected test by using the mean of the diluted and neat results.

FDANov 8, 2004Nationwide• Beckman Coulter Inc

Manitou Bicycle Suspension Forks – Structural Risk (2004)

The recall involves 2005 Manitou Nixon, Stance, and Sherman bicycle suspension forks installed on various high-end mountain bicycles. The Manitou bicycle suspension forks have the model names printed on the sides of the lower leg portions of the fork. Specific models are listed in the table below. 2005 Manitou Nixon Comp, Platinum, Super and Super Plus 145 Suspension Fork Elite 115-145 Suspension Fork Sherman Jumper 110 Suspension Fork Stance Static 80 & 100 Suspension Fork Blunt 100 & 130 Suspension Fork Flow 100-130 Suspension Fork

CPSCNov 8, 2004Nationwide• Answer Products, Inc., of Valencia, CA

Beckman Coulter Inc: DL2000 Data Manager Software, Version 6.4.108

Possibility of reporting an incorrect result occurs due to a software anomally.

FDANov 5, 2004CA, FL, IL +1 more• Beckman Coulter Inc

Cannondale Handlebar Bags – Attachment Failure (2004)

The recall involves 2004 and 2005 models of black handlebar bags. They are the quick-release-type bag, with a support and sleeve to secure it to the bicycle. The "Crossroads" model number is BHB322 and the "Perimeter" model number is BHB320, which can be found on the packaging. The model name and number is not written on the product. The Cannondale logo is on the front of the bags. Only bags with the pattern of reflective material and logo shown below are included in the recall. Older bags that have an American flag sewn into an outer seam or have a "Cannondale Made in USA" tag on an inner seam are not included in the recall.

CPSCNov 5, 2004Nationwide• Cannondale Bicycle Corp., of Bethel, Conn.

Cincinnati Sub-Zero Products: Warm Air Model 135 Warming Units.

Fire/Burn Risk

Burning smell, burned microprocessor board. The firm is modifying the connectors and wiring gauge configuration of the device.

FDANov 5, 2004Nationwide• Cincinnati Sub-Zero Products

Baxter Healthcare Renal Div: Baxter CAPD Solution Transfer Set for use with UV-Flash G...

Disconnection of the tubing at the clamp level of the UV Flash Transfer Set.

FDANov 5, 2004Nationwide• Baxter Healthcare Renal Div

Baxter Healthcare Corp. Rt.: Colleague 3 CX Triple Channel Volumetric Infusion Pumps, ...

A software anomaly causes a failure alarm code 12:303 which audibly alarms and stops the function of all channels in use. This causes an interruption in therapy, which may result in a risk to the patient.

FDANov 4, 2004Nationwide• Baxter Healthcare Corp. Rt.

Brake Parts Cleaner (Valvoline) – Chemical Risk (2004)

The recall involves 13-ounce cans of Pyroil® Non-Chlorinated Brake Parts Cleaner and NAPA® Non-Chlorinated Brake Cleaner. This product is used by professional mechanics as well as "do-it-yourself" consumers who perform brake repairs on their own vehicles. The recalled cans contain one of the following four digits in their date codes, which are found on the bottom of the cans: Pyroil (Part No. 4003) C014 C024 C184 C194 C304 D024 D034 D214 D224 D264 E104 F074 F084 F094 F104 F234 F244 F284 G134 G144 G194 G294 H034 H194 NAPA (Part No. 4800) C024 C094 C184 C194 C224 C234 C304 C314 D014 D034 D054 E054 E064 E144 E244 E254 F174 F184 G284 H124 H304 H314 I074 I084

CPSCNov 4, 2004Nationwide• The Valvoline Company, a Division of Ashland Inc., of Lexington, Ky.

Baxter Healthcare Corp. Rt.: Colleague Single Channel Volumetric Infusion Pumps, produ...

FDANov 4, 2004Nationwide• Baxter Healthcare Corp. Rt.

Hampton Bay Halogen Light Fixture – Safety Issue (2004)

Fire/Burn Risk

The recall involves the Hampton Bay® three-head, flush-mount, halogen light fixture with silver metal rings on the lamp fixtures. It is 15.75 inches wide by 6 inches high. The lights have frosted glass shades. The position of the three lamps on the fixture can be adjusted by turning and bending the lamp heads. A clear label on the fixture reads "MADE IN CHINA," and "E91785."

CPSCNov 4, 2004Nationwide• Cordelia Lighting, of Rancho Dominguez, Calif.