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T.A.G. MEDICAL PRODUCTS CORPORATION, LTD. Kibbutz Gatton GAATON Israel

T.A.G. MEDICAL PRODUCTS CORPORATION, LTD. Kibbutz Gatton GAATON Israel Recalls

All product recalls associated with T.A.G. MEDICAL PRODUCTS CORPORATION, LTD. Kibbutz Gatton GAATON Israel.

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Recall Summary

Total Recalls

1000

Past Year

276

Class I (Serious)

242

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 721–740 of 4099 recalls

Betta Link SR Pronged Guide (TAG Medical) – Surgical Guide Risk (2023)

Drill guides might bend when axial forces are applied by surgeon during procedure and result in potential metal shavings due to friction with the drill bit.Risk to patients includes potential of injury.

FDAMay 4, 2023Nationwide• T.A.G. MEDICAL PRODUCTS CORPORATION, LTD. Kibbutz Gatton GAATON Israel

Betta Link SR Implant Kit (TAG Medical) – Surgical Guide Risk (2023)

FDAMay 4, 2023Nationwide• T.A.G. MEDICAL PRODUCTS CORPORATION, LTD. Kibbutz Gatton GAATON Israel

Immunoassay Premium Level 3 (Randox) – Reporting Delay (2023)

Delay in reporting results due to Quality Controls running high outside of range. Target value and range for ACTH in Immunoassay Premium Level 3, IA2640, lot 2031EC and Immunoassay Premium Control Tri Level kit batch 583135 lot 2031EC has been reassigned on the Roche Cobas e801 due to High recovery outside range

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FDAMay 4, 2023CA, IL, VA +3 more• Randox Laboratories Ltd. 55 Diamond Road Crumlin (North) Ireland

Betta Link LG Pronged Guide (TAG Medical) – Surgical Guide Risk (2023)

FDAMay 4, 2023Nationwide• T.A.G. MEDICAL PRODUCTS CORPORATION, LTD. Kibbutz Gatton GAATON Israel

Betta Link LG Fishmouth Guide (TAG Medical) – Surgical Guide Risk (2023)

FDAMay 4, 2023Nationwide• T.A.G. MEDICAL PRODUCTS CORPORATION, LTD. Kibbutz Gatton GAATON Israel

MRI Biomet Pin Guide (Materialise) – Wrong Guide (2023)

The wrong tibia guide was included intended for a different patient case.

FDAApr 26, 2023Nationwide• Materialise N.V. Technologielaan 15 Heverlee Belgium

Turkey and Havarti Sandwich (Garden Highway) – Undeclared Sesame (2023)

During an internal audit the firm discovered that the label did not declare sesame in their ingredient statement.

Class IIModerate

FDAApr 26, 2023AL, FL, GA +1 more• GARDEN HIGHWAY ATLANTA

DynaDrive Fresh Water Well Pumps (Davey Water) – Electric Shock Risk (2023)

This recall involves the DynaDrive Pumps with model numbers DD60-10NPT and DD90-11NPT and serial numbers between 190791000 and 223365720. The recalled products are water pumps used to stabilize water pressure for fresh water wells. The pumps are constant pressure pumps with an integrated single phase to 3 phase variable speed controller. The pumps have a yellow canister attached to a stainless steel metal casing and aluminum-coated motor. A product identification label sticker is located on the side of the black controller that includes the model and serial number for the unit.

CPSCApr 20, 2023Nationwide• Davey Water Products, of Australia

Single Use Distal Cover (Olympus) - Mucosal Injury Risk (2023)

Fire/Burn Risk

The Single Use Distal Cover MAJ-2315 may cause mucosal injury and/or become detached from the endoscope during use. Consequences of a detached cover could include the risk of aspiration, inhalation, or obstruction that will require urgent removal, and/or burns from an uncovered distal end.

FDAApr 18, 2023Nationwide• Olympus Corporation of the Americas

Flo Smart Water Monitor Battery (Moen) – Fire Hazard (2023)

Fire/Burn Risk

This recall involves the Flo Smart Water Monitor Lithium-Ion Battery Back-Ups. The Flo Water Monitor Battery Backup device was an optional add-on accessory that could be purchased separately to extend certain features of Moen's Flo Smart Water Monitor and Shutoff in the event of a power disruption. Only the battery back-up is being recalled. The dark gray rectangular battery has the FLO logo printed on the lower right-hand side. A sticker showing the status of the light on battery is printed on the lower left-hand side as well as model number 920-001.

CPSCApr 13, 2023Nationwide• Moen Incorporated, of North Olmsted, Ohio

Over-Head Ceiling Tube Support (Shimadzu) - Bolt Fastening Issue (2023)

Eight fixing bolts at the base of the X-ray ceiling tube column assembly may be loose or missing so service is required to install a cable, bracket, and label behind the bracket, indicating when service is required, to eliminate the risk of the device falling.

FDAApr 10, 2023Nationwide• SHIMADZU CORPORATION MEDICAL SYSTEMS DIVISION Nishinokyo Kuwabara Cho Nakagyo-Ku

ViziShot 2 Aspiration Needle (Olympus) – Needle Angle Nonconformance (2023)

Product non-conformance pertaining to the angle of the needle does not meet manufacturing specifications and remained unbent, resulting to slight resistance experienced during needle advancement and retraction.

FDAMar 31, 2023Nationwide• Olympus Corporation of the Americas