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Carroll Healthcare Inc. 1881 Huron St London Canada N6E1P5 Ontario

Carroll Healthcare Inc. 1881 Huron St London Canada N6E1P5 Ontario Recalls

All product recalls associated with Carroll Healthcare Inc. 1881 Huron St London Canada N6E1P5 Ontario.

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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 35441–35460 of 37661 recalls

Carroll Healthcare Inc. 1881 Huron St London Canada N6E1P5 Ontario: Carroll Healthcare brand Spirit bed; models BH2180-111AE,...

The diodes in the control panel may fail, which could result in the thermal breakdown of the circuit board inside of the control box, and cause the bed to cease functioning.

FDAMay 17, 2005Nationwide• Carroll Healthcare Inc. 1881 Huron St London Canada N6E1P5 Ontario

Kydex Glock Holsters (Michaels of Oregon) – Design Flaw (2005)

The recall includes Kydex Belt and Tactical Holsters with thumb break fits for Glock model handguns. The holsters are rigid and are made of black Kydex and come with tension screws for a proper fit. The words, "Uncle Mike's by Michaels of Oregon" are printed on the back of the holster. The recall involves sizes 12, 21, and 25, which is printed on the inside of the holster between the two screws securing the holster to the belt slide.

CPSCMay 17, 2005Nationwide• Michaels of Oregon, of Oregon City, Ore.

LeMaitre Vascular, Inc.: Product is a Pruitt Aortic Occlusion Catheter contained i...

1...1771 177217731774 1775...1884

Page 1773 of 1884Next

LeMaitre Vascular is recalling certain lots of its Pruitt Aortic Occlusion Catheters due to a packaging defect which could compromise product sterility.

FDAMay 17, 2005Nationwide• LeMaitre Vascular, Inc.

Smiths Medical ASD, Inc.: Portex Per-Fit Percutaneous Dilational Tracheostomy Kit ,...

Guiding catheter may have thinner and weaker sidewalls than designed, and may break.

FDAMay 16, 2005Nationwide• Smiths Medical ASD, Inc.

Stryker Howmedica Osteonics Corp.: The TRIO Spondylolisthesis Reduction Instrument is a Clas...

The threaded part of the instrument may break when connected to the screw and potentially result in an adverse health consequence.

FDAMay 16, 2005Nationwide• Stryker Howmedica Osteonics Corp.

Theragenics Corporation: PG910 Spacers, Part number SP101, loaded into Bard Expres...

The spacers loaded in the seeding cartridges were expired and/or the extra loose spacers were labeled with an incorrect expiration date.

FDAMay 16, 2005OH, VA• Theragenics Corporation

Misys Healthcare Systems: Misys Laboratory with Lab Access Results application for ...

Software anomaly may rarely allow modification of previously reported specimen results.

FDAMay 13, 2005Nationwide• Misys Healthcare Systems

Misys Healthcare Systems: Mysis Laboratory version 6.1

When a previously reported microbiology organism result is deleted on a selected patient, reported susceptibilities will not stay with associated organisms and one or more suceptibilities on the culture will be deleted.

FDAMay 10, 2005Nationwide• Misys Healthcare Systems

Biosound Esaote, Inc.: MyLab30CV Ultrasound Imaging System; model 9807300000.

Data may be corrupted upon re-opening archived files.

FDAMay 6, 2005Nationwide• Biosound Esaote, Inc.

Baxter Healthcare Corp. Rt.: Baxter Auto Syringe AS50 Infusion Pump, product code 1M85...

A 'Check Flange' alarm may occur even though the syringe has been properly loaded into the AS50 Infusion Pump. The false alarm may occur during the syringe loading process or while an infusion is running. Also, the occlusion detection and alarm may be delayed when the pumps are used with larger volume syringes at low flow rates.

FDAMay 6, 2005Nationwide• Baxter Healthcare Corp. Rt.

Biosound Esaote, Inc.: MyLab25 Ultrasound Imaging System; Model 9807300002.

Data may be corrupted upon re-opening archived files.

FDAMay 6, 2005Nationwide• Biosound Esaote, Inc.

Dimension Bicycle Stems (Quality Bicycle) – Handlebar Failure (2005)

The recall involves all Dimension-brand road and mountain threadless bicycle stems with a 130 degree rise. The stems are black or silver and have the word "Dimension" painted on the extension. Only models SM2330 to SM2333, SM4555 to SM4558, SM4567, and SM4570 to SM4573 are included in this recall. The model numbers are printed on the original packaging. These handlebar stems all have a 130-degree "high rise" but vary in extension length.

CPSCMay 5, 2005Nationwide• Quality Bicycle Products Inc., of Bloomington, Minn.

Smiths Medical ASD, Inc.: Portex Hypodermic Needle-Pro Syringe & Needle 3mL/LL 25G ...

Mislabeled: Product may contain an incorrect needle size. Product labeled as a 25G x 1" may contain a 25G x 5/8"

FDAMay 5, 2005Nationwide• Smiths Medical ASD, Inc.

Efoora, Inc. dba Virotek, L.L.C.: Virotek SAFELET 1.0 mm Safety Lancets, 1.0 mm depth, st...

The sterility of the lancets may be compromised due to inadequate packaging seals.

FDAMay 5, 2005Nationwide• Efoora, Inc. dba Virotek, L.L.C.

Stryker Howmedica Osteonics Corp.: GMRS Extension Piece, 60 mm; Sterile Stryker Howmedica Os...

Mislabeled package: Package labeled as GMRS Extension Piece 60 mm, lot ZYCOC1 actually contains a GMRS Extension Piece 70 mm extension piece.

FDAMay 5, 2005Nationwide• Stryker Howmedica Osteonics Corp.

Beckman Coulter Inc: Power Processor 3060 Tube Refrigerated Stockyard, P/N 691...

Device does not maintain a uniform internal temperature within 2-8 C at warmer ambient temperatures.

FDAMay 5, 2005Nationwide• Beckman Coulter Inc

Efoora, Inc. dba Virotek, L.L.C.: Virotek SAFELET 2.0 mm Safety Lancets, 2.0 mm depth, st...

The sterility of the lancets may be compromised due to inadequate packaging seals.

FDAMay 5, 2005Nationwide• Efoora, Inc. dba Virotek, L.L.C.

Baxter Healthcare Corp. Rt.: Baxter Sabraset 6060 Administration Set with Pre-attached...

The inlet and outlet lines of the administration set may be reversed, which would result in reverse flow.

FDAMay 4, 2005Nationwide• Baxter Healthcare Corp. Rt.

Lancaster Cribs (Simplicity) – Structural Defect (2005)

Choking Hazard

The recalled cribs are made of wood and painted white. Model numbers 8554W-PT and 8554WW are printed inside the headboard and on the envelope attached to the mattress support. The Simplicity name, address, manufacturing date and model number are written on a label found on the inside bottom of the headboard.

CPSCMay 3, 2005Nationwide• Simplicity Inc., of Reading, Pa. (The firm appears to no longer conduct day to day operations)

Baxter Healthcare Corp. Rt.: Baxter Flo-Gard 6201 Volumetric Infusion Pump, catalog #2...

The mounting screws of the pole clamp may come loose, allowing the pole clamp assembly to detach from the rear pump housing, if they are not maintained on at least an annual basis.

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