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Absorb Health LLC

Absorb Health LLC Recalls

All product recalls associated with Absorb Health LLC.

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Recall Summary

Total Recalls

1000

Past Year

567

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 3201–3220 of 7756 recalls

Advanced Joint Relief Capsules (Absorb Health) – allergen warning (2020)

The firm was notified by the FDA that they failed to included a shellfish allergen on their ingredient panel.

Class IIModerate

FDAApr 15, 2020AZ, CA, FL +14 more• Absorb Health LLC

Estradiol (B & B Pharmaceuticals) – Foreign Material Risk (2020)

cGMP deviations: Presence of foreign material (Teflon)introduced at the production level.

Class IIModerate

FDAApr 14, 2020Nationwide• B & B Pharmaceuticals, Inc.

Ivoclar Vivadent AG Benderer Strasse 2 Schaan Liechtenstein: Ivoclar Vivadent IPS e.max ZirCAD CER/inLab LT A1 C17/5 -...

Restorations crack during the sintering process.

1...159 160161162 163...388

Page 161 of 388Next

FDA

Apr 13, 2020

Nationwide

• Ivoclar Vivadent AG Benderer Strasse 2 Schaan Liechtenstein

Baxter Healthcare Corporation: Prismaflex Control Unit

Prismaflex product code 114870 does not have FDA regulatory clearance and was inadvertently distributed.

FDAApr 7, 2020PR• Baxter Healthcare Corporation

C.A. Greiner & Sohne Gesellschaftmbh Greiner St. # 70 Kremsmunster Austria: VACUETTE Blood Transfer Unit. Lot no. A19024NX. Expiratio...

While transferring blood the needle may dislodged and remain in the tube stopper which may cause needle stick injury or blood leakage.

FDAApr 3, 2020Nationwide• C.A. Greiner & Sohne Gesellschaftmbh Greiner St. # 70 Kremsmunster Austria

Abbott Laboratories: Accelerator APS Aliquoter Module, List number: 07L40 - Pr...

In the case of an AQM clot detection error a portion of the distilled water from the Aliquoter Module hydraulic circuit may be dispensed into the Primary Tube leading to sample dilution, which could lead to incorrect results.

FDAApr 2, 2020Nationwide• Abbott Laboratories

Abbott Laboratories: ARCHITECT C Peptide Calibrator - Product Usage: used as a...

Error in the renewal documentation process for license in Mexico. All in date ARCHITECT C Peptide Reagents, Calibrators and Controls are being recalled until a new license is obtained.

FDAApr 1, 2020IN• Abbott Laboratories

Abbott Laboratories: ARCHITECT C Peptide Reagent - Product Usage: used as an a...

Error in the renewal documentation process for license in Mexico. All in date ARCHITECT C Peptide Reagents, Calibrators and Controls are being recalled until a new license is obtained.

FDAApr 1, 2020IN• Abbott Laboratories

Beckman Coulter Inc.: iQ200 Series Urine Microscopy Analyzer- All part numbers

A defect in the SATA power adapter cable within the instrument s computer has the potential risk for an electrical short that may lead to the following outcomes: charring and/or melting of the SATA adapter cable within the computer s metal enclosure, smoke emanating from PC6, flames contained within PC6, or an inability to use the device s CD-ROM.

FDAMar 30, 2020Nationwide• Beckman Coulter Inc.

Boston Scientific Corporation: MoXy Laser Fiber, Material Number 0010-2400 - Product Usa...

To reinforce existing instructions within the Directions for Use (DFU) and provide further guidance which will be added to the DFU that may reduce the likelihood of metal cap and fiber tip break temperature related complaints.

FDAMar 30, 2020Nationwide• Boston Scientific Corporation

Beckman Coulter Inc.: iChemVELOCITY Urine Chemistry System-

A defect in the SATA power adapter cable within the instruments computer has the potential risk for an electrical short that may lead to the following outcomes: charring and/or melting of the SATA adapter cable within the computers metal enclosure, smoke emanating from PC6, flames contained within PC6, or an inability to use the devices CD-ROM.

FDAMar 30, 2020Nationwide• Beckman Coulter Inc.