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THREAD COUNSEL INC DBA LAWS OF MOTION

THREAD COUNSEL INC DBA LAWS OF MOTION Recalls

All product recalls associated with THREAD COUNSEL INC DBA LAWS OF MOTION.

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Recall Summary

Total Recalls

1000

Past Year

567

Class I (Serious)

25

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 2981–3000 of 7756 recalls

THREAD COUNSEL INC DBA LAWS OF MOTION: LOM Disposable Surgical Gowns/Medical Gowns, Single-Use

Medical gowns distributed to customers did not include appropriate labeling, and some gowns may not meet FDA's standards for surgical gowns.

FDASep 17, 2020IN, NY• THREAD COUNSEL INC DBA LAWS OF MOTION

Boston Scientific Corporation: Hurricane RX Biliary Balloon Dilatation Catheter Catalog ...

RX tunnel component (black sheath) may detach from the catheter shaft due to lower bond strength.

FDASep 16, 2020Nationwide• Boston Scientific Corporation

Nymalize (Arbor Pharmaceuticals) – Subpotent Drug (2020)

Subpotent Drug

FDASep 16, 2020

1...148 149150151 152...388

Page 150 of 388Next

Nationwide

• Arbor Pharmaceuticals Inc.

Bien-Air Surgery Sa rue de l' ouest 2b Le Noirmont Switzerland: Entellus Medical REF SSA-102 SN ******* Shaver System Foo...

The magnet located inside the foot pedal may come off and may result in unattended start of unstoppable motor.

FDASep 11, 2020Nationwide• Bien-Air Surgery Sa rue de l' ouest 2b Le Noirmont Switzerland

Bien-Air Surgery Sa rue de l' ouest 2b Le Noirmont Switzerland: Stryker Instruments REF 5452-007-000 SN ******* S2 MINI ...

The magnet located inside the foot pedal may come off and may result in unattended start of unstoppable motor.

FDASep 11, 2020Nationwide• Bien-Air Surgery Sa rue de l' ouest 2b Le Noirmont Switzerland

Bien-Air Surgery Sa rue de l' ouest 2b Le Noirmont Switzerland: Bien-Air Surgery REF 1600686-001 SN ******* OSSEOSTAP Foo...

The magnet located inside the foot pedal may come off and may result in unattended start of unstoppable motor.

FDASep 11, 2020Nationwide• Bien-Air Surgery Sa rue de l' ouest 2b Le Noirmont Switzerland

Bien-Air Surgery Sa rue de l' ouest 2b Le Noirmont Switzerland: Bien-Air Surgery REF 1600517-001 SN ******* MULTIFUNCTION...

The magnet located inside the foot pedal may come off and may result in unattended start of unstoppable motor.

FDASep 11, 2020Nationwide• Bien-Air Surgery Sa rue de l' ouest 2b Le Noirmont Switzerland

Bien-Air Surgery Sa rue de l' ouest 2b Le Noirmont Switzerland: Bien-Air Surgery REF 1600407-001 SN **** FOOTCTRL OSSEODO...

The magnet located inside the foot pedal may come off and may result in unattended start of unstoppable motor.

FDASep 11, 2020Nationwide• Bien-Air Surgery Sa rue de l' ouest 2b Le Noirmont Switzerland

RTI Surgical, Inc. (dba Pioneer Surgical Technology, Inc.): Streamline MIS Navigation System Taps, Catalog numbers ...

The Streamline MIS Navigation System taps are not compatible with the Streamline MIS tap sleeve.

FDASep 11, 2020IN, MI• RTI Surgical, Inc. (dba Pioneer Surgical Technology, Inc.)

2019 WABASH NATIONAL VAN Recall: EQUIPMENT

Wabash National Corporation (Wabash) is recalling certain 2019-2021 Van trailers manufactured with flat bottom floors that are equipped with aerodynamic skirts. The aerodynamic skirts attached to the van trailers may come loose.

NHTSASep 10, 2020Nationwide• WABASH NATIONAL

Citalopram Oral Solution (PAI Holdings) – Impurity Specification Failure (2020)

Failed Impurities/Degradation Specifications; high out of specification results obtained at the 9 month stability timepoint

FDASep 9, 2020Nationwide• PAI Holdings, LLC. dba Pharmaceutical Associates Inc

Braxton Medical Corporation: B. Braun Introcan IV Safety Catheters, sterile - Product ...

Recalled products do not have FDA approval for sale in the United States.

FDASep 4, 2020Nationwide• Braxton Medical Corporation

AB ULAX Merkuriusgatan 8 Motala Sweden: 1500 Flex Heat and Moisture Exchanger, Catalog Reference ...

Firm has received 6 complaints that the Heat Moisture Exchanger (HME) disconnected from the closed respiratory circuit during use. If the HME separates, the ventilator circuit may not provide adequate ventilation to the patient, potentially resulting in lack of oxygen leading to hypoxia or death.

FDASep 4, 2020Nationwide• AB ULAX Merkuriusgatan 8 Motala Sweden

PITTSBURGH AUTOMOTIVE A/C MANIFOLD GAUGE SET Equipment Recall: EQUIPMENT

Harbor Freight Tools (Harbor Freight) is recalling certain Pittsburgh Automotive A/C R134A Manifold Gauge Sets, part number 62707, sold between May 22, 2020 and August 11, 2020. The labels for the high pressure and low pressure manifold and coupler valves may have been swapped, incorrectly stating which way to open or close the valves.

NHTSASep 1, 2020Nationwide• PITTSBURGH AUTOMOTIVE

Brainlab AG Olof-palme-str. 9 Munich Germany: Ultrasound Navigation Software 1.0 and Ultrasound Integra...

Brainlab Ultrasound Navigation Software does not support the modification of the probe's image width.

FDAAug 31, 2020Nationwide• Brainlab AG Olof-palme-str. 9 Munich Germany

Blanxart Congo Chocolate Bar (Culinary Collective) – Foreign Object (2020)

A foreign object found by a consumer in a chocolate bar.

Class IIModerate

FDAAug 27, 2020IL, IN, NY +1 more• Power Selles Imports dba Culinary Collective

Beckman Coulter Inc.: BECKMAN COULTER ACCESS Immunoassay Systems - Access Uncon...

Due to alkaline phosphatase (ALP) associated interference causing falsely elevated uE3 (Unconjugated Estriol assay) results.

FDAAug 26, 2020Nationwide• Beckman Coulter Inc.

Boston Scientific Corporation: Opticross 35 15 MHz Peripheral Imaging Catheter 8F (2.74 ...

Opticross 35 Peripheral Imaging Catheter is being recalled because the incremental telescoping length markings near the proximal end of the catheter shaft can flake off when the device is manipulated. No patient harm has been reported to date. The most common potential adverse health consequence would be prolonged procedure to exchange the catheter for another as this potential issue is observable and has occurred outside of the patient's body. The most server health consequence that is reasonably expected to occur if a catheter with this potential issue is used is embolization which would result of the flaking marks advance while flushing the catheter. All recalled devices should be returned to Boston Scientific.

FDAAug 24, 2020Nationwide• Boston Scientific Corporation

Irvine Biomedical Inc, a St. Jude Medical Co.: Inquiry Steerable Diagnostic Catheter, REF: IBI-81104 - P...

Steerable diagnostic catheter packages labeled Model IBI-81104, batch 7397352 incorrectly contained Model IBI-87002, batch 7397307. Packages labeled Model IBI-87002, batch 7397307 incorrectly contained Model IBI-81104, batch 7397352.If physicians fail to observe the catheter difference, the intracardiac electrograms will not be representative of the desired signals, could result in procedure delay

FDAAug 24, 2020Nationwide• Irvine Biomedical Inc, a St. Jude Medical Co.

Brainlab AG Olof-palme-str. 9 Munich Germany: Cirq Arm System - Model SBS 1.3.2 (Art.No. 56000-01B) and...

Holding force of the Positioning Arm can be reduced by prolonged non-use.

FDAAug 20, 2020IL, OH, DC• Brainlab AG Olof-palme-str. 9 Munich Germany