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Abbott Laboratories, Inc

Abbott Laboratories, Inc Recalls

All product recalls associated with Abbott Laboratories, Inc.

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Recall Summary

Total Recalls

1000

Past Year

566

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 6461–6480 of 7756 recalls

Abbott Laboratories, Inc: ARCHITECT i1000SR" Processing Module System For In Vitro ...

During manufacturing, two components of the ARCHITECT i1000SR were reversed which could potentially cause falsely elevated patient results due to a sample-reagent and reagent-sample carryover.

FDAOct 21, 2008CO, FL, GA +11 more• Abbott Laboratories, Inc

Bio-Rad Laboratories Inc: Bio-Rad Variant II TURBO Hemoglobin Testing System with C...

Sample results may be assigned to the wrong barcode number and tube position numbers, leading to discrepant sample results.

FDAOct 17, 2008Nationwide• Bio-Rad Laboratories Inc

Spacelabs Healthcare, Incorporated: Intesys Clinical Suite (ICS) G2 92810 Smart Disclosure. ...

Potential for device to print out the wrong waveform data for the time indicated in the printout or display.

FDA

1...322 323324325 326...388

Page 324 of 388Next

Oct 17, 2008

• Spacelabs Healthcare, Incorporated

Beckman Coulter Inc.: Access Peristaltic Pump component of: UniCel DxI 800 Acce...

The recall was initiated after Beckman Coulter confirmed reports of a new premature failure of the upper aspirate peristaltic pump in the systems listed above. Premature failure of the pump may negatively affect precision. The failure is limited to those UniCel DXI 800, DXI 600, and DxC 880i systems which have a pump identified with one of the new pump manufacturing numbers (Mfg. Nos.) listed ab

FDAOct 9, 2008Nationwide• Beckman Coulter Inc.

Boston Scientific Corporation: Atlantis PV Peripheral Imaging Catheter, model number H74...

Product is mislabeled as having a shelf life of 3 years, where the actual shelf life is 1 year.

FDAOct 9, 2008PR• Boston Scientific Corporation

Nerf N-Strike Blasters (Hasbro) – skin catch (2008)

This recall involves the Nerf N-Strike Recon CS-6 Blasters for children age 6 and up. The toy blaster is yellow with a black handle and orange plunger, trigger, and reload clip. The word "NERF" in black lettering is on both sides of the blaster and the word "ARMED" is indented on the orange plunger. "RECON CS-6" is on the gray cocking mechanism. There are five interchangeable parts including the shoulder stock, the flip-up sight, barrel extension, quick re-load clip and dual-mode light beam. Model number 63552 and UPC codes 653569272021 and 653569311218 can be found on the packaging. Only blasters with an exposed orange plunger are included in this recall.

CPSCOct 9, 2008Nationwide• Hasbro Inc., of Pawtucket, R.I.

Boston Scientific Corporation: Excelsior SL-10 Microcatheter, placed in sterile pouch. ...

Packaging issue may result in failure to maintain sterile barrier.

FDAOct 7, 2008Nationwide• Boston Scientific Corporation

Boston Scientific Corporation: Boston Scientific Easy Core" Biopsy System, 18 ga. x 10 c...

Boston Scientific Corporation initiated a recall of its easy Core" BIOPSY SYSTEM due to difficulty cocking or arming the cannula latch on the device. This difficulty may result in an inability to use the device.

FDAOct 7, 2008Nationwide• Boston Scientific Corporation

Mindray DS USA, Inc., dba Datascope Patient Monitoring: AS3000 Anesthesia Delivery System. Datascope Patient Mon...

Two issues have been identified with the AS3000 unit. 1. The threadlocker of the caster (wheels) may not have been utilized, which may allow the caster to loosen and possibly separate from the unit. 2. The use of select brands of pre-pack absorber in the absorber canister of the AS3000 has been associated, in some cases, with gas leakage around the pre-pack, rather than through the absorber mate

FDAOct 7, 2008CA, IN• Mindray DS USA, Inc., dba Datascope Patient Monitoring

BioSense Webster, Inc. Circuito Interior Norte, # 1820 Parque Industrial Salvarcar Cd. Juarez, Chihuahua Mexico: Biosense Webster NaviStar RMT Diagnostic/Ablation Steerab...

Biosense Webster initiated the recall because of the potential concern with one of the Printed Circuit Board (PCB) components used in the NaviStar RMT Catheters, which may cause the ablation catheter icon to shift on the map viewer when RF energy is being applied. Therefore the user, attempting a linear ablation in the location displayed on the CARTO RMT screen, may ultimately apply RF energy to u

FDAOct 2, 2008CA, CT, FL +24 more• BioSense Webster, Inc. Circuito Interior Norte, # 1820 Parque Industrial Salvarcar Cd. Juarez, Chihuahua Mexico

C. R.Bard, Inc./BardElectrophysiology Division: 7F Bard SSV 13 cm Split Sheath with Valve and sideport Ca...

Failure to insert the guidewire through the introducer needle.

FDAOct 1, 2008Nationwide• C. R.Bard, Inc./BardElectrophysiology Division

Toshiba American Medical Systems Inc: Toshiba Infinix fluoroscopy DFP-8000D Digital Radiography...

Audible signal is not available at all times when using the HLC fluoroscopy mode. Special means of activation are not designed in for selection of High Level Controls, as required by regulation.

FDASep 29, 2008Nationwide• Toshiba American Medical Systems Inc

Alcon Laboratories, Inc.: PurePoint System Operator's Manual, Catalog Number 806575...

Alcon had identified that indications for use unapproved by the Food and Drug Administration are included in the PurePoint Laser System Operator's Manual, Catalog Number 8065751131, Revision B.

FDASep 26, 2008CA, CO, CT +14 more• Alcon Laboratories, Inc.

Ski-Doo Snowmobiles (BRP) – Drive Axle Failure (2008)

This recall involves Ski-Doo® Model Year 2008 and 2009 snowmobiles. Models included in the recall are listed below. Model numbers are printed on the side panels of the snowmobiles. Ski-Doo® Model Year 2008 MXZ X 800R PowerTEK MXZ X 600HO SDI MXZ Adrenaline 800R PowerTEK MXZ Adrenaline 600HO SDI MXZ TNT 500SS MXZ Trails 500SS GSX Limited Touring 600HO SDI GSX Limited 800R PowerTEK GSX Limited 600HO SDI GSX Sport 500SS MXZ Renegade X 800R PowerTEK MXZ Renegade X 600HO SDI MXZ Renegade 800R PowerTEK MXZ Renegade 600HO SDI Summit X 800R Power TEK Summit Everest 800R PowerTEK MXZ X 600RS Ski-Doo® Model Year 2009 MXZ TNT 600HO E-TEC

CPSCSep 26, 2008Nationwide• Bombardier Recreational Products Inc., of Valcourt, Canada

Bd Diagnostic Systems Tripath: BD PrepStain System, Model Number: 799-14000-00; Catalog ...

Software Error in the non-gyn program of some devices may cause non-gyn samples to be incorrectly transferred from centrifuge tubes to slides potentially result in mismatched patient results.

FDASep 26, 2008Nationwide• Bd Diagnostic Systems Tripath

Abbott Laboratories Inc.: ABBOTT Clinical Chemistry Bilirubin Calibrator, List Numb...

The field action was initiated after an investigation for the Total Bilirubin reagents (List Number 8G62 and List Number 6L45) determined that the matrix of the secondary standard used in the value assignment of the calibrator is sensitive to the Diazo method. The matrix of this secondary standard caused a positive bias. Because of these findings, a new Total Bilirubin calibrator value assignm

FDASep 12, 2008Nationwide• Abbott Laboratories Inc.

Beckman Coulter Inc.: Access Immunoassay Systems Assay Protocol File (APF) Soft...

The recall was initiated because Beckman confirmed a customer report that a timing conflict can occur while aspirating samples for the Access Total BhCG assay.

FDASep 11, 2008Nationwide• Beckman Coulter Inc.

Gas Boilers (PB Heat) – carbon monoxide risk (2008)

Fire/Burn Risk

This recall involves the DE and PSC II Gas Fired Cast Iron Boilers with the Endura Plastics Model ES2035 pressure switch used for home heating and domestic hot water heating. The boilers were available in either natural or LP gas. The boiler rating label is located on the top jacket panel on Series PSCII models and the left side jacket panel on the Series DE models. The label includes the model and serial number. The following model names and serial numbers are included in the recall: Model Name Serial Number DE-03, DE-04, DE-05 and DE-06 5040768 to 5052860 PSCII-03, PSCII-04, PSCII-05, and PSCII-06 5040777 to 5052166 Other suffix designation may follow the base model number, such as SV-WPC.

CPSCSep 11, 2008Nationwide• PB Heat LLC, of Bally, Pa.

Barcoview 35 President Kennedy Park Kortrijk Belgium: Barco Surgical Display, Model MDSC-2124 The 24-inch MDSC...

The front protective cover may loosen and completely fall off.

FDASep 9, 2008Nationwide• Barcoview 35 President Kennedy Park Kortrijk Belgium

Abbott Laboratories, Inc: ACCELERATOR APS Centrifuge Module (Hettich Robotic centri...

ACCELERATOR APS Centrifuge Module being recalled due to potential for micro-cracks to form over time in the metal centrifuge rotor buckets that may cause the centrifuge buckets to disconnect from the rotor in the centrifuge during centrifugation.

FDASep 9, 2008Nationwide• Abbott Laboratories, Inc