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The Anspach Effort, Inc.

The Anspach Effort, Inc. Recalls

All product recalls associated with The Anspach Effort, Inc..

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Recall Summary

Total Recalls

1000

Past Year

593

Class I (Serious)

65

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 9441–9460 of 10391 recalls

The Anspach Effort, Inc.: "REF BLU-395 mm Fluted Acorn. Use with B-BLUE-S Att...

Laceration Risk

The Anspach Effort, Inc. initiated a recall on May 6, 2008 for their Sterile Bone Cutting Burrs. All affected customers were notified of the recall by letter dated 5/29/2008.

FDAMay 19, 2008Nationwide• The Anspach Effort, Inc.

The Anspach Effort, Inc.: "REF TURQ-L55 mm Fluted Ball. Use with B-TURQ-L A...

Laceration Risk

The Anspach Effort, Inc. initiated a recall on May 6, 2008 for their Sterile Bone Cutting Burrs. All affected customers were notified of the recall by letter dated 5/29/2008.

FDAMay 19, 2008Nationwide• The Anspach Effort, Inc.

The Anspach Effort, Inc.: "REF LHD-6B-M6 mm Fluted Ball. Use with LONG-HD Att...

Laceration Risk

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The Anspach Effort, Inc. initiated a recall on May 6, 2008 for their Sterile Bone Cutting Burrs. All affected customers were notified of the recall by letter dated 5/29/2008.

FDAMay 19, 2008Nationwide• The Anspach Effort, Inc.

The Anspach Effort, Inc.: "REF QD8-5B5 mm Fluted Ball. Use with QD8 Attachmen...

Laceration Risk

The Anspach Effort, Inc. initiated a recall on May 6, 2008 for their Sterile Bone Cutting Burrs. All affected customers were notified of the recall by letter dated 5/29/2008.

FDAMay 19, 2008Nationwide• The Anspach Effort, Inc.

The Anspach Effort, Inc.: 'REF SIL-3-101.93 mm Suture Pass Drill/ 1.17 eye. U...

Laceration Risk

The Anspach Effort, Inc. initiated a recall on May 6, 2008 for their Sterile Bone Cutting Burrs. All affected customers were notified of the recall by letter dated 5/29/2008.

FDAMay 19, 2008Nationwide• The Anspach Effort, Inc.

The Anspach Effort, Inc.: "REF L-CRN2.5 mm x 25.4 mm Fluted Router. Use with...

Laceration Risk

The Anspach Effort, Inc. initiated a recall on May 6, 2008 for their Sterile Bone Cutting Burrs. All affected customers were notified of the recall by letter dated 5/29/2008.

FDAMay 19, 2008Nationwide• The Anspach Effort, Inc.

The Anspach Effort, Inc.: "REF A-CRN1.85 mm x 16 mm Fluted Router. Use with ...

Laceration Risk

The Anspach Effort, Inc. initiated a recall on May 6, 2008 for their Sterile Bone Cutting Burrs. All affected customers were notified of the recall by letter dated 5/29/2008.

FDAMay 19, 2008Nationwide• The Anspach Effort, Inc.

The Anspach Effort, Inc.: "REF GRE-11.85 mm x 16 mm Fluted Router. Use with B...

Laceration Risk

The Anspach Effort, Inc. initiated a recall on May 6, 2008 for their Sterile Bone Cutting Burrs. All affected customers were notified of the recall by letter dated 5/29/2008.

FDAMay 19, 2008Nationwide• The Anspach Effort, Inc.

The Anspach Effort, Inc.: "REF S-35DC3.5 mm Coarse Diamond Ball, Extended Len...

Laceration Risk

The Anspach Effort, Inc. initiated a recall on May 6, 2008 for their Sterile Bone Cutting Burrs. All affected customers were notified of the recall by letter dated 5/29/2008.

FDAMay 19, 2008Nationwide• The Anspach Effort, Inc.

The Anspach Effort, Inc.: "REF QD11-6B6 mm Fluted Ball. Use with QD11 Attachm...

Laceration Risk

The Anspach Effort, Inc. initiated a recall on May 6, 2008 for their Sterile Bone Cutting Burrs. All affected customers were notified of the recall by letter dated 5/29/2008.

FDAMay 19, 2008Nationwide• The Anspach Effort, Inc.

The Anspach Effort, Inc.: "REF S-6AC6 mm Fluted Acorn. Use with SHORT Attachm...

Laceration Risk

The Anspach Effort, Inc. initiated a recall on May 6, 2008 for their Sterile Bone Cutting Burrs. All affected customers were notified of the recall by letter dated 5/29/2008.

FDAMay 19, 2008Nationwide• The Anspach Effort, Inc.

The Anspach Effort, Inc.: "REF BLU-LS9-5E4.7 mm x 20 mm Fluted Drum, Side Cut...

Laceration Risk

The Anspach Effort, Inc. initiated a recall on May 6, 2008 for their Sterile Bone Cutting Burrs. All affected customers were notified of the recall by letter dated 5/29/2008.

FDAMay 19, 2008Nationwide• The Anspach Effort, Inc.

FireX CO/Smoke Alarms (Maple Chase) – alarm malfunction (2008)

The recall includes FireX branded 10000 and 12000 series alarms with item numbers: 10000, 12000, 12000C, 12000-6, 12200, 12220, 12400, 12400C manufactured between June 1, 2007 and February 1, 2008. The date code appears on the back of the unit with a four-digit year, three-digit month followed by the day (ex: 2007JUN1 for June 1, 2007). Units with a manufacture date code prior to June 1, 2007 are not included in this recall.

CPSCMay 15, 2008Nationwide• Maple Chase Company, of Plain City, Ohio

Shindaiwa Backpack Blowers (Shindaiwa) – injury hazard (2008)

Laceration Risk

This recall involves Shindaiwa Models EB8510 and EB8510RT. All models up to serial # 7014728 are included. The backpack blowers weigh approximately 24 pounds and include Serial Numbers through February 2007 production (S/N 702XXXX) which are located on the side label. These machines are black and blue with a red and black label that reads, "EB8510, Shindaiwa."

CPSCMay 15, 2008Nationwide• Shindaiwa Kogyo Co. Ltd, of Hiroshima, Japan

Hitachi Medical Systems America Inc: EUB-9500/HI VISION 8500 Diagnostic Ultrasound Scanners, ...

The firm's parent company discovered a DICOM UID (Universal Identifier) code mix-up which can occur due to a software error. This error can cause the images from two (2) different patient scans to become intermingled and consequently, labeled incorrectly.

FDAMay 12, 2008AR, CA, IN +1 more• Hitachi Medical Systems America Inc

Hitachi Medical Systems America Inc: EUB-6500/HI VISION 6500 Diagnostic Ultrasound Scanners, D...

The firm's parent company discovered a DICOM UID (Universal Identifier) code mix-up which can occur due to a software error. This error can cause the images from two (2) different patient scans to become intermingled and consequently, labeled incorrectly.

FDAMay 12, 2008AR, CA, IN +1 more• Hitachi Medical Systems America Inc

GE Healthcare Integrated IT Solutions: GE Centricity AW Suite 2.0 Software running on the Centri...

Incorrect measurement of the aortic length in certain cases of aneurysm during the use of the aorta protocol or customized protocol of the Centricity AW Suite 2.0 running on the Centricity RA 1000 or RA600/CA1000 workstations.

FDAMay 9, 2008Nationwide• GE Healthcare Integrated IT Solutions

Deluxe Bottle Warmers (Munchkin) – Fire Hazard (2008)

This recall involves the Munchkin Deluxe Bottle and Food Warmer with Pacifier Cleaning Basket 2-in-1 Design, model #13301 and lot number TP-1487. The product is used to warm food and bottles of various sizes. The set includes a main basket, a lift-out basket, an adapter ring, and a measuring cup. "Munchkin" is located on the front of the warmer and "TP-1487" is located on the bottom. Only warmers bearing lot number "TP-1487" are included in this recall.

CPSCMay 8, 2008Nationwide• Munchkin Inc., of North Hills, Calif.

GE Healthcare Integrated IT Solutions: GE Centricity PACS RA1000 Workstation; for diagnostic ima...

A software anomaly results in incorrect study date and time information being displayed in the report screen and title, which may result in a potential patient misdiagnosis.

FDAMay 6, 2008Nationwide• GE Healthcare Integrated IT Solutions

Michigan Orthopaedic Products, Inc.: InterGro DBM Demineralized Bone Matrix in a lipid carrier...

Exposure to temperature extremes -- Product was not stored under controlled conditions and may have been temperature abused. Exposure to temperature extremes could cause problems with device safety (e.g. risk of infection) or problems with device effectiveness (e.g. lower healing rates if the factors or collagen in the device were affected by the temperature extremes).

FDAMay 5, 2008Nationwide• Michigan Orthopaedic Products, Inc.