Stay Informed

Get email alerts when new recalls match your interests.

Recall data is updated hourly from official government sources. Very recent recalls may not yet appear. About our data sources

About

We make U.S. recall data searchable and accessible for consumers and businesses.

Site

FAQ
Browse by State
Statistics
Recall Classifications
About
Enterprise API

Legal

Privacy Policy
Terms of Service
Report Incorrect Info

Official Sources

FDA Recalls ↗
USDA FSIS ↗
CPSC Recalls ↗
NHTSA Recalls ↗

RSS Feed

Home
/
Brands
/
Abbott Laboratories MPG

Abbott Laboratories MPG Recalls

All product recalls associated with Abbott Laboratories MPG.

Get alerts for this brand

Recall Summary

Total Recalls

1000

Past Year

567

Class I (Serious)

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 7221–7240 of 7756 recalls

Abbott Laboratories MPG: ARCHITECT Folate Reagent Kit, list 6C12-20 ( 4 x 100 test...

concentrations for normal samples generated with current reagent lots of the ARCHITECT Folate assay are lower than data generated for the package insert.

FDAMar 11, 2005Nationwide• Abbott Laboratories MPG

Baxter Healthcare Corp. Rt.: Clinician Workstation Software, product code 2M5042

The medication administration results displayed in the 'View Results' link may be inaccurate.

FDAMar 10, 2005CA, MA, MO +1 more• Baxter Healthcare Corp. Rt.

Abbott Health Products, Inc.: IMx HAVAB Controls In Vitro Test

Abbott identified through investigational studies that IMxHAVAB Controls lot 21059Q100 is generating Negative Control values outside the upper range specified in the IMxHAVAB Package Insert.

FDA

1...360 361362363 364...388

Page 362 of 388Next

Mar 4, 2005

Nationwide

• Abbott Health Products, Inc.

Baxter Healthcare Corp. Rt.: Baxter Extension Sets with PosiFlow Access Device for IV ...

Inadequate directions for use resulting in fluid leaks, valves sticking in the open position, and flow output restriction.

FDAMar 3, 2005Nationwide• Baxter Healthcare Corp. Rt.

Baxter Healthcare Corp. Rt.: Baxter PosiFlow Access Device for IV Access; product code...

Inadequate directions for use resulting in fluid leaks, valves sticking in the open position, and flow output restriction.

FDAMar 3, 2005Nationwide• Baxter Healthcare Corp. Rt.

Baxter Healthcare Corp. Rt.: Configuration Transfer Cable; an accessory for the Collea...

The Configuration Tranfer Cable for the Colleague Infusion Pumps has incorrect thumb screws on it., not allowing firm connections of the cable to the pump to transfer data to the biomedical engineer's diagnostic device.

FDAMar 2, 2005Nationwide• Baxter Healthcare Corp. Rt.

Baxter Healthcare Corp. Rt.: Baxter ClearLink Intravenous (IV) Solution Sets and Exte...

Possible occlusion of the Clearlink injection site valve due to inadequate silicone lubrication of the slit in the upper seal of the valve.

FDAFeb 28, 2005Nationwide• Baxter Healthcare Corp. Rt.

Abbott Laboratories, Inc: ARCHITECT c800 for Conventional Units and for SI Units, V...

Device has incorrect notation associated with therapeutic drug monitoring assays.

FDAFeb 28, 2005AZ, CA, IL +9 more• Abbott Laboratories, Inc

Farm Teether Rattle (Tiffany) – Child Safety Risk (2005)

Laceration Risk

The recalled rattle is designed for children ages 3 months and up. The Farm Teether Rattle is a hollow, sterling silver ring approximately 3 inches in diameter with a bar across its center. The bar is attached to the interior of the ring at two points and has three farm animals (sheep, duck and cow) and two beads that rotate on the bar. Small plastic beads inside the ring rattle when the product is shaken. Inscribed on the rattle is "© 2002 TIFFANY & CO. 925."

CPSCFeb 25, 2005Nationwide• New England Sterling of Attleboro, Mass., for Tiffany and Company of New York, N.Y.

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

Swelling of the sealed lead-acid batteries in the infusion pump can cause internal pump damage, and excessive battery discharge can damage the batteries if the pump is left on battery power for an extended period of time after teh Battery Depleted alarm occurs.

FDAFeb 25, 2005Nationwide• Baxter Healthcare Corp. Rt.

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

FDAFeb 25, 2005Nationwide• Baxter Healthcare Corp. Rt.

Boston Scientific Corporation: Vaxcel Low Profile Port with PASV Valve and 6F Polyuretha...

Potential separation of the port base from the port cover after implantation.

FDAFeb 25, 2005IN• Boston Scientific Corporation

Buoyancy Compensators (Cressi-sub) – Diving Equipment Issue (2005)

Buoyancy Compensator devices provide buoyancy control for scuba divers by allowing them to inflate or deflate the devices. The recalled buoyancy compensators have model numbers J107, J113, J115, and J119. The numbers appear on the top right-hand corner of the unit (on the shoulder). "CRESSI" is written on the buoyancy control devices.

CPSCFeb 23, 2005Nationwide• Cressi-sub S.p.A., of Genoa, Italy

Beckman Coulter Inc: Access Immunoasay Systems Digoxin Reagent

Variability in results on Patient and QC results of 20-25%, high and low.

FDAFeb 23, 2005Nationwide• Beckman Coulter Inc

Bicycle Suspension Seat Post (Cannondale) – Structural Weakness (2005)

The recall involves Lee Chi model 1-X bicycle suspension seat posts. The seat post was manufactured by a component manufacturer for Cannondale and installed on various 2005 model year Cannondale brand bicycles. These seat posts have a natural anodized aluminum finish, a 1-X logo is laser etched on the outer tube, and a black, yellow and red instruction booklet with the 1-X logo is attached. Lee Chi is also known as Promax, but the seat posts are not marked with either name. Specific Cannondale bicycle models with affected seat posts are listed in the table below. Model names are printed on the top tube of the bicycle frame. 2005 Cannondale Bicycle Models Adventure 800 Comfort 600 Feminine Adventure 800 Feminine Road Warrior 800 Adventure 600 Sport Road 1000 Adventure 600 Feminine Sport Road 800 Comfort 800 Sport Road 500 Comfort 800 Feminine Touring 2000 Comfort 600

CPSCFeb 18, 2005Nationwide• Cannondale Bicycle Corporation, of Bethel, Conn.

Log Splitter (Brave Products) – Equipment Defect (2005)

The log splitters are made of steel and painted orange and black. They have trailer hitches and rubber tires. Each log splitter has a decal on the side that reads "Brave Products, Inc." and "__ ton" (either 15, 22, 26, or 34). The following models are being recalled: Brave VH0234 (34 ton) Serial #S012368 through S016976 Brave VH9926 (26 ton) Serial #S014226 through S017534 Brave VH9922 (22 ton) Serial #S011460 through S016862 Brave HB0115 (15 ton) Serial #S013853 through S017534 (Serial number plate is located on the hydraulic tank)

CPSCFeb 15, 2005Nationwide• Brave Products Inc., Streator, Ill.

Baxter Healthcare Corp. Rt.: Baxter I-Pump Pain Management System infusion pump, produ...

Potential failures of the pump due to upstream occlusion alarms, electro-static discharge, system error 32 or 33, history printout errors and fluid volume in 'Use Previous Rx' when priming through the pump.

FDAFeb 10, 2005Nationwide• Baxter Healthcare Corp. Rt.

Ski-Doo Snowmobiles (Bombardier) – electrical issue (2005)

2005 Ski-Doo Mach Z 995 and Summit 995 snowmobiles without functional electric starter. Recalled models are listed below in this table: Year Model Package Model Number 2005 Mach Z Adrenaline™ AB5A Summit Highmark CA5A / CA5B Highmark X CD5A / CD5B / CD5C

CPSCFeb 9, 2005Nationwide• Bombardier Recreational Products Inc., of Quebec, Canada

Girls' Cardigan Sweater (H&M) – safety concern (2005)

The recalled cardigan sweaters are black with a black faux fur trim around the wrists, neck and down the front center of the sweater. The sweaters were sold in girls' sizes 7Y through 14Y and are made of 100 percent acrylic. "Dubbster" and RN number "0101255" are printed on the inside neck label of the sweaters.

CPSCFeb 4, 2005Nationwide• Dubbster (H & M private label), H & M, of New York, N.Y.

Greer Laboratories Inc: Sterile Empty Vials for Allergenic Extracts, 100ml size

Product may not be sterile.

FDAJan 28, 2005AZ, CA, FL +14 more• Greer Laboratories Inc