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Anabolic Science Labs, LLC

Anabolic Science Labs, LLC Recalls

All product recalls associated with Anabolic Science Labs, LLC.

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Recall Summary

Total Recalls

1000

Past Year

433

Class I (Serious)

138

Most Recent

Dec 2025

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 5541–5560 of 7663 recalls

Slim X Lean Hour Energy (Anabolic Science Labs) – Undeclared Hormone (2014)

Undeclared Allergen

This product is being recalled due to the presence of undeclared synthetic hormone/prohormone (methylated anabolic steroid) ingredient.

Class IIModerate

FDADec 8, 2014Nationwide• Anabolic Science Labs, LLC

Zimmer Manufacturing B.V.: Trilogy¿ Fiber Metal Acetabular Shell Size 54 mm OD Th...

Zimmer received a single complaint wherein a Trilogy® Fiber Metal Multi-Hole Acetabular Shell would not attach to the inserter/impactor instrumentation. Subsequent investigation found the polar-hole threads to be present but non-conforming to specifications, in that the minor diameter was undersized. Investigation also indicates that the issue is isolated and affects only lot 62714305, which

Class IIModerate

FDADec 4, 2014Nationwide• Zimmer Manufacturing B.V.

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Simvastatin Tablets 20mg (Micro Labs) – Impurity Specification (2014)

Failed Impurities/Degradation Specifications: Product failed a known impurity specification.

Class IIILow

FDADec 4, 2014Nationwide• Micro Labs Usa, Inc S

Simvastatin Tablets 80mg (Micro Labs) – Impurity Specification (2014)

Failed Impurities/Degradation Specifications: Product failed a known impurity specification.

Class IIILow

FDADec 4, 2014Nationwide• Micro Labs Usa, Inc S

Orthovita, Inc., dBA Stryker Orthobiologics.: Stryker Orthobiologics Imbibe Aliquot Needle Bone Cement ...

There is the potential for a breach in the inner or outer packaging pouches of all lots of the Stryker Orthobiologics Imbibe Aliquot Needle Bone Cement Needle.

Class IIModerate

FDADec 4, 2014Nationwide• Orthovita, Inc., dBA Stryker Orthobiologics.

Orthovita, Inc., dBA Stryker Orthobiologics.: Stryker Orthobiologics Imbibe Bone Marrow Aspiration Need...

There is the potential for a breach in the inner or outer packaging pouches of all lots of the Imbibe Bone Marrow Aspiration Needle.

Class IIModerate

FDADec 4, 2014Nationwide• Orthovita, Inc., dBA Stryker Orthobiologics.

Simvastatin Tablets 40mg (Micro Labs) – Impurity Specification (2014)

Failed Impurities/Degradation Specifications: Product failed a known impurity specification.

Class IIILow

FDADec 4, 2014Nationwide• Micro Labs Usa, Inc S

2015 MERCEDES BENZ SPRINTER 2500 Recall: ENGINE AND ENGINE COOLING:ENGINE:DIESEL

Fire/Burn Risk

Mercedes-Benz USA, LLC - DBA Sprinter (Mercedes) is recalling certain model year 2014-2015 Sprinter 2500, and Sprinter 3500 vehicles manufactured February 28, 2014, to November 21, 2014. In the affected vehicles, oil may leak from around the chain tensioner gasket area.

NHTSADec 1, 2014Nationwide• MERCEDES BENZ

2015 MERCEDES-BENZ GLK250 Recall: ENGINE AND ENGINE COOLING:ENGINE:DIESEL

Fire/Burn Risk

Mercedes-Benz USA, LLC (Mercedes) is recalling certain model year 2014-2015 E250 BlueTec, E250 BlueTec 4Matic, GLK250 4Matic BlueTec, and 2015 ML250 4Matic BlueTec vehicles manufactured February 28, 2014, to November 10, 2014. In the affected vehicles, oil may leak from around the chain tensioner gasket area.

NHTSADec 1, 2014Nationwide• MERCEDES-BENZ

Getinge Disinfection Ab: GETINGE 46-SERIES Medical Washer-Disinfector, Models 46-4...

Getinge Disinfection AB received complaints regarding sediment residuals in the manifold of the washer and disinfector of Getinge 46-Series (CM302) with PACS 300/350 control. After performing detailed root cause analysis, the firm has identified the problem as insufficient water flow throughout the manifold due to formation of air pockets where sedimentation may occur.

Class IIModerate

FDANov 26, 2014Nationwide• Getinge Disinfection Ab

Utility Vehicle Doors (Pro Armor) – Impact Risk (2014)

Laceration Risk

This recall involves Pro Armor doors sold as accessories for model year 2010 through 2014 Polaris RZR 800 and RZR 900 models. The doors have a black powder coated finish and have four major components: a large square sheet metal panel, a smaller triangular sheet metal panel, a tubular metal frame and a latch. The panels are interchangeable and come in two styles. One style has cutout vents along the top and the other style has none. The smaller panel has a white Pro Armor logo below the cutouts. The door frame has the logo and "Pro Armor" on the top tube. The latch is silver with a black locking mechanism that attaches to the vehicle frame and a handle that attaches to the door.

CPSCNov 25, 2014Nationwide• LSI Products Inc. dba Pro Armor, Riverside, Calif.

Dasani Purified Water (Coca Cola Bottling) – potential mold (2014)

An equipment malfunction during production that may have led to the appearance of mold in some product.

Class IIILow

FDANov 24, 2014AL, FL, GA +1 more• Coca Cola Bottling Company United, LLC

Zimmer Manufacturing B.V.: Bone Screw, self-tapping The Trilogy shells are availabl...

Analysis of returned complaint devices, product in inventory, and device manufacturing records has identified tool marks isolated to one specific machining mill to be the cause of the fractures. .

Class IIModerate

FDANov 21, 2014Nationwide• Zimmer Manufacturing B.V.

Cyberonics, Inc: Cyberonics VNS Therapy AspireHC, Model 105 Generator. The...

The recalled product was distributed with an incorrect serial number printed on the device's label.

Class IIModerate

FDANov 20, 2014PA• Cyberonics, Inc

Clark Laboratories, Inc. (dba,Trinity Biotech USA): Trinity biotech Captia (TM) Syphilis IgM Capture Test Kit...

Through in-house routine real time stability monitoring of Trinity's Captia Syphilis IgM Capture Test Kit, Lot 033, the firm identified a failure of the kit to meet its labeled expiry dating of 6 months.

Class IIILow

FDANov 17, 2014CA, FL, NY +1 more• Clark Laboratories, Inc. (dba,Trinity Biotech USA)

MAYHEM Capsules (Chaotic Labz) – Undeclared Ingredients (2014)

Undeclared Allergen

Marketed Without An Approved NDA/ANDA: FDA analysis found this product to contain undeclared dexamethasone and cyproheptadine which are FDA approved drugs making this product an unapproved drug.

Class IIModerate

FDANov 14, 2014Nationwide• Chaotic Labz

2011 STARCRAFT BUS QUEST Recall: EQUIPMENT ADAPTIVE/MOBILITY

Forest River, Inc. (Forest River) is recalling certain 2010-2012 Starcraft Bus Quest and Prodigy school buses manufactured January 13, 2010, to November 17, 2011 equipped with certain model S2005, S2010, S5005, S5010, S5505, and S5510 wheelchair lifts manufactured by Ricon Corporation. The platform side plate of the affected wheelchair lifts may crack.

NHTSANov 13, 2014Nationwide• STARCRAFT BUS

Tankless Gas Water Heaters (Daesung Celtic) – Fire risk (2014)

Fire/Burn Risk

This recall involves all models of single- and dual-purpose Coaire and Quietside brand tankless gas water heaters. The recalled water heaters heat either 4 or 7.2 gallons of water per minute. They are white and come in the following dimension ranges: 25-28 inches tall x 15-19 inches wide x 8-14 inches thick. The words "S-Line Condensing" are on the top front and brand names "Coaire" or "Quietside" are on the bottom front of the recalled water heaters.

CPSCNov 13, 2014Nationwide• Daesung Celtic Enersys Co. Ltd., of Chungbuk, Korea

Air Exchangers (Venmar Ventilation) – Fire hazard (2014)

Fire/Burn Risk

This recall involves air exchangers with and without heat recovery sold under different brands that are used to circulate air in and out of the home. The metal air exchangers are painted blue or grey. Air exchangers with heat recovery included in this recall were manufactured from January 2002 through May 2008 and have brand and model information written on a silver or black label on the outside panel. Air exchangers without heat recovery included in this recall were manufactured from January 2002 through July 2009 and have brand and model information printed on the unit's rating plate or imprinted on the side of the unit. The following brand names and model numbers are included in the recall: Brand Model Number The "X" can be either a letter or a number. Bryant Carrier Day and Night Payne ERVBBLHAXXXX ERVBBLHUXXXX ERVCCLHAXXXX ERVCCLHUXXXX HRVBBLHAXXXX HRVBBLHUXXXX HRVBBLVUXXXX HRVBBSVUXXXX HRVCCLHAXXXX HRVCCLHUXXXX, HRVCCLVUXXXX HRVCCSVUXXXX VA3AAXXXX VB5AAXXXX VC5AAXXXX VL3AAA0XX Conformax Flair Guardian by Broan NuTone Venmar Venmar AVS Venmar Klima 0XX 100X 160XXXX 1.X 1XX 2.X 3XX 40X 4XXXX 30 30XX 30XXX 55 55XX 85115 AE 60 AEXX C32042 CH 30110 EA-109 EA-20XXX EARC ER-40XXX ERVX00HC HRVX00H IVL XXX NUTR 130 PRO XXX RC-120 VA-80 VA-30000 VE-25 Frigidaire Maytag Partners Choice Tappan Westinghouse 91871X Heil HRV XX5 XRC Husch vänEE 10 100X 1XX 160XXXX 20 20XX, 30XX 43XXX 45XXX 48405 90 Protech Rheem Rudd Weatherking 84-XRVX00 Sears Optimum York 5263554X000

CPSCNov 13, 2014Nationwide• Venmar Ventilation Inc., of Quebec, Canada

2007 STARCRAFT BUS STARQUEST Recall: EQUIPMENT ADAPTIVE/MOBILITY

Forest River, Inc. (Forest River) is recalling certain model year 2006-2012 Starcraft Bus Xpress, Starquest, Starlite, Allstar, Allstar XL, MVP, Ultrastar, and XLT transit buses manufactured June 1, 2006, to February 27, 2012 equipped with certain model S2005, S2010, S5005, S5010, S5505, and S5510 wheelchair lifts manufactured by Ricon Corporation. The platform side plate of the affected wheelchair lifts may crack.

NHTSANov 13, 2014Nationwide• STARCRAFT BUS