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Jordache Ltd., of New York, N.Y.

Jordache Ltd., of New York, N.Y. Recalls

All product recalls associated with Jordache Ltd., of New York, N.Y..

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Recall Summary

Total Recalls

1000

Past Year

742

Class I (Serious)

175

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 10401–10420 of 11123 recalls

U.S. Polo Hooded Sweatshirts (Jordache) – Strangulation Risk (2006)

The recalled youth hooded fleece garments have drawstrings. They were sold in a variety of colors and have "U.S. Polo Assn." written on them. A sewn-in tag also reads, "U.S. Polo Assn". The style number for these garments is 12-5169.

CPSCMar 15, 2006Nationwide• Jordache Ltd., of New York, N.Y.

Kimberly-Clark Corporation: Kimberly Clark * Facet Block Tray * Single Use * Sterile ...

Procedural Trays may contain extension sets that do not meet USP specification requirements for non pyrogenicity (less than or equal to 2.25 EU/device (Endotoxin Units/device).

FDAMar 15, 2006Nationwide• Kimberly-Clark Corporation

Kimberly-Clark Corporation: Kimberly Clark * Nerve Block Tray * Single Use * Sterile ...

Procedural Trays may contain extension sets that do not meet USP specification requirements for non pyrogenicity (less than or equal to 2.25 EU/device (Endotoxin Units/device).

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FDAMar 15, 2006Nationwide• Kimberly-Clark Corporation

Beckman Coulter Inc: Unicel DxC 600/800 SYNCHRON Clinical Systems; Operating S...

It was confirmed that the ORDAC (Over Range Detection And Correction) feature (auto & manual) does not perform correctly for the glucose cup chemistry (GLUCm) when sample type of 'Other' is selected w/operating software versions 1.0 & 1.2. Results for these samples could be elevated as much as twice the actual value. The ORDAC feature does function properly w/serum, plasma, urine & CSF.

FDAMar 15, 2006Nationwide• Beckman Coulter Inc

Kimberly-Clark Corporation: Kimberly Clark * 20' Minibore Extension Line * Single Use...

There exists a possibility that the Pain Management Procedural Trays may contain extension sets that do not meet USP specification requirements for non pyrogenicity (less than or equal to 2.25 EU/device (Endotoxin Units/device).

FDAMar 15, 2006Nationwide• Kimberly-Clark Corporation

Kimberly-Clark Corporation: Kimberly Clark * Nerve Root Block Tray * Single Use * Ste...

Procedural Trays may contain extension sets that do not meet USP specification requirements for non pyrogenicity (less than or equal to 2.25 EU/device (Endotoxin Units/device).

FDAMar 15, 2006Nationwide• Kimberly-Clark Corporation

Beckman Coulter Inc: SYNCHRON LX 20, SYNCHRON LX 20 PROClinical Systems; Opera...

It was confirmed that the ORDAC (Over Range Detection And Correction) feature (auto & manual) does not perform correctly for the glucose cup chemistry (GLUCm) when sample type of 'Other' is selected w/operating software version 4.5. Results for these samples could be elevated as much as twice the actual value. The ORDAC feature does function properly w/serum, plasma, urine & CSF.

FDAMar 15, 2006Nationwide• Beckman Coulter Inc

Kimberly-Clark Corporation: Kimberly Clark * Universal Block Tray * Single Use * Ster...

Procedural Trays may contain extension sets that do not meet USP specification requirements for non pyrogenicity (less than or equal to 2.25 EU/device (Endotoxin Units/device).

FDAMar 15, 2006Nationwide• Kimberly-Clark Corporation

Beckman Coulter Inc: SYNCHRON LX i 725 Clinical Systems; Operating Software Ve...

It was confirmed that the ORDAC (Over Range Detection And Correction) feature (auto & manual) does not perform correctly for the glucose cup chemistry (GLUCm) when sample type of 'Other' is selected w/operating software version 4.5. Results for these samples could be elevated as much as twice the actual value. The ORDAC feature does function properly w/serum, plasma, urine & CSF.

FDAMar 15, 2006Nationwide• Beckman Coulter Inc

Elekta, Inc.: PrecisePLAN 2.10 Treatment Planning System

Error in dose rates which were calculated at exactly twice the expected values.

FDAMar 15, 2006IL, NY, PA +1 more• Elekta, Inc.

Kimberly-Clark Corporation: Kimberly Clark * Selective Nerve Block Tray * Single Use ...

Procedural Trays may contain extension sets that do not meet USP specification requirements for non pyrogenicity (less than or equal to 2.25 EU/device (Endotoxin Units/device).

FDAMar 15, 2006Nationwide• Kimberly-Clark Corporation

Stryker Howmedica Osteonics Corp.: Trident PSL Acetabular Shell;Arc Deposited;Hydroxylapatit...

Dimensional anomaly

FDAMar 13, 2006Nationwide• Stryker Howmedica Osteonics Corp.

Karl Storz Endoscopy America Inc 600 Corporate Pointe: Storz Documentation Cart with Articulating Arm, Model Num...

THE ARTICULATING ARM ON THE CART, WHICH HOLDS THE MONITOR, MAY FALL OFF FROM THE CART DURING MANIPULATION. WHEN IT FALLS, IT COULD HIT THE GROUND OR FALL ON THE PEOPLE/OBJECTS THAT ARE IN CLOSE PROXIMITY.

FDAMar 10, 2006Nationwide• Karl Storz Endoscopy America Inc 600 Corporate Pointe

Forever-Glo Nite Lites (AmerTac) – Fire Hazard (2006)

Fire/Burn Risk

The recalled "Forever-Glo Nite Lites™" look like small picture frames that plug into the wall. Only model numbers 75001 or 75002 with a manufacture date of April 2004 or later are included in this recall. Model 75001 is white or bronze-colored and has molded scroll-work around the front of the nite lite. "Model 75001" is printed on the back of the nite lite. Model 75002 is silver-colored and has a punched tin frame. "Model C8A5" is printed on the back. Both nite lite models measure about 3 inches by 3 inches and are about ¼ inch thick. "AmerTac™" and a circle with the month and year of manufacture are indicated on the back of the nite lites.

CPSCMar 8, 2006Nationwide• American Tack & Hardware Co. Inc. (AmerTac), of Saddle River, N.J.

Cook Urological, Inc.: Cook Harrison fetal bladder stent set, sterile; REF J-HFB...

Instructions for Use (IFU) booklet missing pages 5-12. Pages 5-8 in English; 9-12 in Danish, describe stent duration, patient preparation, assembly, implanting, follow-up and removal instructions. IFU, device description, indications, contraindications, warnings, precautions, patient counseling, clinical usage, clinical study data, adverse events. One patient booklet lacked pages 3-6, & 55-58.

FDAMar 1, 2006Nationwide• Cook Urological, Inc.

Little Tikes Animal Flashlights – Lead Paint (2006)

The Glowin' Dino Flashlight and the Glowin' Doggy Flashlight are about 9 inches long and make an electronic sound when switched on. The green dinosaur roars, and the white and brown dog barks. Only flashlights with the following date codes are included in the recall: LC5H161, LC5H291, LC5I031, LC5I091, LC5I131, LC5J061, LC5J231, and LC5J311. The date codes are found on the bottom of the flashlights. Units that do not contain these codes or other animal flashlight characters made by The Little Tikes Co. are not included in this recall. Also, units that have an "R" at the end of the date code are not included in the recall.

CPSCMar 1, 2006Nationwide• The Little Tikes Co., of Hudson, Ohio

Youth Hooded Fleece (Next Marketing) – Strangulation Risk (2006)

The recalled youth hooded fleece garments have drawstrings. They were sold in a variety of colors and many of them have the names of colleges and universities printed or embroidered on them. A sewn-in tag reads, "Lil Fan" or "LF 2."

CPSCFeb 24, 2006Nationwide• Next Marketing Inc., of Wabash, Ind.

Stryker Howmedica Osteonics Corp.: Triathlon X3 UHMWPE Tibial Inserts and Patellar Component...

Stryker Orthopaedics became aware of a potential anomaly related to the packaging process of referenced lots of X# polyethylene used on Scorpio, Triathlon and Trident inserts.

FDAFeb 17, 2006Nationwide• Stryker Howmedica Osteonics Corp.

Depuy Mitek, a Johnson & Johnson Co.: Depuy Mitek Bioknotless Anchor with Ethibond Suture Ref N...

The inserter shafts bend, as they were manufactured with a different stainless steel than specified.

FDAFeb 17, 2006Nationwide• Depuy Mitek, a Johnson & Johnson Co.

Stryker Howmedica Osteonics Corp.: Scorpio X3 UHMPWE Tibial Inserts and Scorpio X3 UHMWPE Pa...

Stryker Orthopaedics became aware of a potential anomaly related to the packaging process of referenced lots of X# polyethylene used on Scorpio, Triathlon and Trident inserts.

FDAFeb 17, 2006Nationwide• Stryker Howmedica Osteonics Corp.