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Contract Pharmaceuticals Limited Canada

Contract Pharmaceuticals Limited Canada Recalls

All product recalls associated with Contract Pharmaceuticals Limited Canada.

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Recall Summary

Total Recalls

1000

Past Year

304

Class I (Serious)

34

Most Recent

Nov 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 661–680 of 4747 recalls

Clindamycin Phosphate Solution (Contract Pharma) – Leaking Container (2023)

Defective Container: slow leakage under the cap

FDAAug 23, 2023Nationwide• Contract Pharmaceuticals Limited Canada

Apellis Injection Kit (Apellis) – Needle Characteristic Deviation (2023)

19-gauge x 1" inch filter needles showed appearances of a small fraction of non-preferred characteristics. A causal relationship has not been established between the structural variations in this 19-gauge filter needle and the rare events of retinal vasculitis

FDAAug 22, 2023Nationwide• Apellis Pharmaceuticals, Inc.

Trandolapril/Verapamil Tablets (Glenmark) – subpotent medication (2023)

Subpotent: Out of Specification for Assay Test at the 3-month time point.

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FDAAug 14, 2023Nationwide• Glenmark Pharmaceuticals Inc., USA

VITROS Chemistry Proboscis Assembly (Ortho-Clinical) – Manufacturing Issue (2023)

Ortho Clinical Diagnostics (QuidelOrtho) confirmed certain Proboscis/Piston Assemblies manufactured between 07-Apr-2022 (Date code: 040722) and 19-Dec-2022 (Date code: 121922) may not perform as intended due to an out-of-specification barrel component. This may cause VITROS VersaTips and/or VITROS MicroTips to be improperly seated on the proboscis, which may result in falsely elevated Gentamicin and Valproic Acid assay results as well as an increased frequency of condition codes resulting in delayed patient results. The issue was identified by internal testing when reported instruments failed to pass release testing and were traced to the molded Proboscis part J56639 with date codes from 040722 onward.

FDAAug 9, 2023Nationwide• Ortho-Clinical Diagnostics, Inc.

Activator Concentrate (Ecometics) – manufacturing deviation (2023)

CGMP Deviations: Products not manufactured under current good manufacturing practices.

Class IIModerate

FDAAug 9, 2023Nationwide• Ecometics, Inc.

Alcolado Relampago (Ecometics) – CGMP Manufacturing Issues (2023)

CGMP Deviations: Products not manufactured under current good manufacturing practices.

Class IIModerate

FDAAug 9, 2023Nationwide• Ecometics, Inc.

AstrinGyn (Ecometics) – CGMP Manufacturing Issues (2023)

CGMP Deviations: Products not manufactured under current good manufacturing practices.

Class IIModerate

FDAAug 9, 2023Nationwide• Ecometics, Inc.

Yager's Liniment (Ecometics) – CGMP Manufacturing Issues (2023)

CGMP Deviations: Products not manufactured under current good manufacturing practices.

Class IIModerate

FDAAug 9, 2023Nationwide• Ecometics, Inc.

Lugol's Iodine Solution (Ecometics) – manufacturing deviation (2023)

CGMP Deviations: Products not manufactured under current good manufacturing practices.

Class IIModerate

FDAAug 9, 2023Nationwide• Ecometics, Inc.

Blis-To-Sol Liquid (Ecometics) – CGMP Manufacturing Issues (2023)

CGMP Deviations: Products not manufactured under current good manufacturing practices.

Class IIModerate

FDAAug 9, 2023Nationwide• Ecometics, Inc.

Unguentine Ointment (Ecometics) – CGMP Manufacturing Issues (2023)

CGMP Deviations: Products not manufactured under current good manufacturing practices.

Class IIModerate

FDAAug 9, 2023Nationwide• Ecometics, Inc.

ADVIA Chemistry Iron Reagents (Siemens) – QC Result Bias (2023)

There is a potential for a positive bias on Quality Control (QC) and patient sample results when using some IRON_2 reagent wedge pairs. When the issue occurs, the observed bias will vary wedge to wedge.

FDAAug 8, 2023Nationwide• Siemens Healthcare Diagnostics, Inc.

VITROS XT ALKP Slides (Ortho-Clinical) – Substrate Depletion (2023)

Samples containing high levels of ALKP (or an interfering substance) could deplete the available substrate in the reagent layer of a VITROS ALKP Slide and not post the substrate deleption (DP) code, which may result in the System reporting an incorrect value (lower than the actual value), which may result in missed or delayed diagnosis of liver disease.

FDAAug 5, 2023Nationwide• Ortho-Clinical Diagnostics, INc.

VITROS XT TBIL-ALKP Slides (Ortho-Clinical) – Substrate Depletion (2023)

Samples containing high levels of ALKP (or an interfering substance) could deplete the available substrate in the reagent layer of a VITROS ALKP Slide and not post the substrate deleption (DP) code, which may result in the System reporting an incorrect value (lower than the actual value), which may result in missed or delayed diagnosis of liver disease.

FDAAug 5, 2023Nationwide• Ortho-Clinical Diagnostics, INc.

Tobramycin Ophthalmic Solution (Alembic) – Impurity Specifications (2023)

Failed Impurities/Degradation Specifications

FDAJul 27, 2023Nationwide• ALEMBIC PHARMACEUTICALS, INC.

ADVIA Chemistry Protein Test (Siemens) – reagent carryover (2023)

There is a potential for ADVIA Chemistry Urinary/Cerebrospinal Fluid Protein reagent carryover impacting Enzymatic Creatinine_2 (ECRE_2). Falsely depressed ECRE_2 results may be observed when the assay is processed after the UCFP test on ADVIA Chemistry systems.

FDAJul 25, 2023Nationwide• Siemens Healthcare Diagnostics, Inc.

Fentanyl-Bupivacaine Solution (SCA Pharma) – Rejected Units Shipped (2023)

cGMP deviations: due to shipment of rejected units.

Class IIModerate

FDAJul 20, 2023KY, NJ• SCA Pharmaceuticals

Dofetilide Capsules (Sun Pharma) – Content Uniformity Issue (2023)

Out of Specification result observed in content uniformity testing

FDAJul 18, 2023Nationwide• SUN PHARMACEUTICAL INDUSTRIES INC

Copan Transfer Pipette (Copan) – Aspiration Defect (2023)

Due to plastic defects, the pipette aspiration capability potentially doesn't meet the expected tolerance

FDAJul 14, 2023CA• Copan Diagnostics Inc

Gas-Fired Hot Water Boilers (ECR International) – Carbon monoxide risk (2023)

This recall involves gas-fired hot water residential boilers with brand names Dunkirk, Utica Boilers, Utica Heating, Pennco, Green Mountain and Columbia and with model numbers DXL-K, MGB-K, UH15B-K, 15B-K, GMGW-K, or MCB-K respectively. The boilers are blue and/or gray in color, 32 inches tall, 13 to 27 inches wide and 26 inches deep. The model and serial numbers are located on the boiler rating plate in the front left corner of the top panel. The following models and serial numbers are included in the recall: Brand Name Boiler Model Number Serial Number Range Dunkirk DXL-K: DXL-060K DXL-095K DXL-120K DXL-150K DXL-175K DXL-205K DXL-235K Serial Number Range: 392201652s thru 402202738s 012302567s and 012302571s Utica Boilers MGB-K: MGB-060K MGB-095K MGB-120K MGB-150K MGB-175K MGB-205K MGB-235K Serial Number Range: 402200481s thru 402202693s 012302268s thru 012302566s Columbia MCB-K: MCB-060K MCB-095K MCB-120K MCB-150K MCB-175K MCB-235K Serial Number Range: 402201449s thru 402202214s Utica Heating UH15B-K: UH15B-060K UH15B-095K UH15B-120K UH15B-150K UH15B-175K UH15B-235K Serial Number Range: 392201654s thru 402202800s 012302274s thru 012303099s Pennco 15B-K: 15B-060K 15B-095K 15B-120K 15B-150K 15B-175K 15B-235K Serial Number Range: 392202597s thru 402202806s 012301918s thru 012303055s Green Mountain GMGW-K: GMGW-060K GMGW-095K GMGW-120K GMGW-150K GMGW-175K GMGW-235K Serial Number Range: 392201653s thru 402202686s 012301924s thru 012301961s

CPSCJul 13, 2023Nationwide• ECR International Inc., of Utica, New York