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lab921, Seattle, Wash.

lab921, Seattle, Wash. Recalls

All product recalls associated with lab921, Seattle, Wash..

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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 6601–6620 of 7756 recalls

Starbucks Fusion Coffee Mugs (lab921) – burn hazard (2007)

Fire/Burn Risk

This recall involves two styles of Starbucks 14-ounce Fusion Coffee Mugs. The mugs are white and have a black plastic handle, and a stainless steel base. The cups have "Starbucks Coffee" printed on a black stamp or a brown original Starbucks logo stamp.

CPSCDec 6, 2007Nationwide• lab921, Seattle, Wash.

Ventlab Corporation: Ventlab-assembled Anesthesia breathing bags. The recall i...

During setup and potentially during procedures, the breathing bag can become separated from the taped bushing that is part of the breathing bag assembly.

FDADec 5, 2007IL• Ventlab Corporation

Boston Scientific Corporation: Pathway Balloon Expandable Ureteral Access Sheath- 11/14/...

Sheath Removal Difficulty: Users experience difficulty in removing the sheath.

1...329 330331332 333...388

Page 331 of 388Next

FDA

Nov 30, 2007

Nationwide

• Boston Scientific Corporation

Baxter Healthcare Corp. Rt.: Baxter Single Day INFUSOR Portable Elastomeric Infusion S...

Leaking: leaks at the tubing flow restrictor connection to either the coupler or the male luer during filling.

FDANov 29, 2007Nationwide• Baxter Healthcare Corp. Rt.

Baxter Healthcare Renal Div: HomeChoice PRO Automated Peritoneal Dialysis Systems; Cat...

Unrecorded Infusion; If the system is powered down or a power failure occurs during a fill cycle, the HomeChoice system may not record the last 1-4 pump strokes infused into the patient when the power is restored. This situation may create a potential unrecorded delivery of approximately 15-60 mL of fluid being infused into the patient.

FDANov 20, 2007Nationwide• Baxter Healthcare Renal Div

Baxter Healthcare Renal Div: Baxter HomeChoice Automated Peritoneal Dialysis Systems; ...

FDANov 20, 2007Nationwide• Baxter Healthcare Renal Div

Baxter Healthcare Renal Div: Baxter Renal Software Suite v.3.0 and v.3.1 - Renal Link ...

Pre-Treatment/Post-Treatment Report errors: 1) The Heparin Bolus Value is displayed on Pre and Post Treatment Reports for patients with "No Heparin" orders (RenalSoft v2.0, Renal Software Suite v.3.0 and v.3.1), and 2) Withheld Medications are incorrectly displayed as Administered on the Pre-Treatment report (RenalSoft v.2.0 only).

FDANov 14, 2007PR• Baxter Healthcare Renal Div

Baxter Healthcare Renal Div: Baxter RenalSoft v.2.0 Patient Management Software Suite ...

FDANov 14, 2007PR• Baxter Healthcare Renal Div

Bio-Rad Laboratories Inc: BioRad BioPlex 2200 Software, for BioPlex 2200 Instrument...

Incorrect values: An error was found in the BioPlex 2200 Software, Version 2.0 that results in assignment values being utilized for the BioPlex assay Calibrator Set that may be slightly different from those printed on the Value Assignment Data Sheet. Some values may be identical between the lot assignment combinations with the ANA Screen with MDSS kit.

FDANov 13, 2007Nationwide• Bio-Rad Laboratories Inc

Bio-Rad Laboratories: BIOPLEX 2200 EBV IgG KIT, CALIBRATORS, AND CONTROLS: 100 ...

False negative results due to reagent packs exhibiting low signal.

FDANov 13, 2007Nationwide• Bio-Rad Laboratories

Bio-Rad Laboratories: BIOPLEX 2200 EBV IgM KIT, CALIBRATORS, AND CONTROLS: 100 ...

False negative results due to reagent packs exhibiting low signal.

FDANov 13, 2007Nationwide• Bio-Rad Laboratories

Football Helmet Chin Straps (Nike) – Injury Risk (2007)

The recalled football helmet chin strap consists of a plastic cup with a foam liner, straps and four metal snaps. They were sold in both youth and adult sizes and come in black/gray and white/gray color combinations. The Nike Swoosh trademark is printed on the outside of the chin cup and DRI-FIT™ is printed on the foam liner. "Made in China" and one of the following four style numbers is printed on the inside of the strap: FA0016 046, FA0016 130, FA0021 046, or FA0021 130.

CPSCNov 13, 2007Nationwide• Nike Inc., of Beaverton, Ore.

Bio-Rad Laboratories: BIOPLEX 2200 MULTI-ANALYTE DETECTION SYSTEM: a) 100 test ...

False negative results due to reagent packs exhibiting low signal.

FDANov 13, 2007Nationwide• Bio-Rad Laboratories

Bio-Rad Laboratories: BIOPLEX 2200 SYPHILIS IgG Kit: 100 tests - Catalog No. 66...

False negative results due to reagent packs exhibiting low signal.

FDANov 13, 2007Nationwide• Bio-Rad Laboratories

Toshiba American Medical Systems Inc: Xario; SSA-660A; software version 1.0 and later

Toshiba America Medical System Inc initiated a field corrective action on Aplio 50; SSA-700A; software version 5.5r002 and later, Aplio 80; SSA-700A; software version 5.5r002 and later, and Xario; SSA-660A; software version 1.0 and later, because the product does not meet the Safety Standard requirements.

FDANov 12, 2007Nationwide• Toshiba American Medical Systems Inc

Brainlab AG Ammerthalstrasse 8 Kirchheim B. Muenchen Germany: VectorVision (VV) Sky Navigation Platform (19" Computer R...

Diameter of cables used for installation are to small for the applied current. If an internal short circuit is produced the medical power supply will not shut down automatically and will continue to deliver current, which could result in overheating cables.

FDANov 12, 2007Nationwide• Brainlab AG Ammerthalstrasse 8 Kirchheim B. Muenchen Germany

Toshiba American Medical Systems Inc: Aplio 50; SSA-700A; software version 5.5r002

FDANov 12, 2007Nationwide• Toshiba American Medical Systems Inc

Toshiba American Medical Systems Inc: Aplio 80; SSA-770A; software version 5.5r002

FDANov 12, 2007Nationwide• Toshiba American Medical Systems Inc

Convertible Cribs (Goodbaby) – Entrapment Risk (2007)

This recall involves Wendy Bellissimo Collection convertible cribs, model numbers 5945-0521 and 5545-0521, sold in honey and cherry finishes. The full size cribs have a sleigh design and one of the following purchase order numbers at the bottom rail of the headboard: 272903, 272904, 273904, 276728, 276729, 291081, 323975, 324472, 320318, 323976, 332883 365620, 368466 in honey, and 338535, 338537 and 332884 in cherry. All other Wendy Bellissimo Collection cribs are not involved in this recall.

CPSCNov 8, 2007Nationwide• Goodbaby Child Products Company Ltd., of China

Nova Biomedical Corporation: Nova - EZ CHEM Linearity Solution P/N 9618, Nova Biomedic...

Incorrect Results - Creatinine results were lower than the laboratory reference method.

FDANov 2, 2007Nationwide• Nova Biomedical Corporation