DrugSep 23, 2020
RLC Labs WP Thyroid, Westhroid Pure, 2 Grain (130 mg) Thyroid USP recall — FDA D-1613-2020
CGMP Deviations: manufactured under the same conditions as those found to be subpotent.
Class IIFDA: TerminatedRLC Labs Inc.
Latest records
Latest recalls — page 970
The newest recall records with useful source details are listed here.
DrugSep 23, 2020
RLC Labs WP Thyroid, Westhroid Pure, 3/4 Grain (48.75 mg) Thyroid USP recall — FDA D-1608-2020
CGMP Deviations: manufactured under the same conditions as those found to be subpotent.
Class IIFDA: TerminatedRLC Labs Inc.
DrugSep 23, 2020
RLC Labs Nature-Throid, Thyroid USP [liothyronine (T3) 20.25 mcg and levothyroxine (T4) 85.5 recall — FDA D-1603-2020
CGMP Deviations: manufactured under the same conditions as those found to be subpotent.
Class IIFDA: TerminatedRLC Labs Inc.
DrugSep 23, 2020
RLC Labs Nature Throid, 1.25 Grain (81.25 mg) Thyroid USP [Liothyronine (T3) 11.25 mcg recall — FDA D-1617-2020
Subpotent Drug: FDA analysis found product to be subpotent
Class IFDA: TerminatedRLC Labs Inc.
DrugSep 23, 2020
RLC Labs Nature-Throid, Thyroid USP [liothyronine (T3) 22.5 mcg and levothyroxine (T4) 95 recall — FDA D-1604-2020
CGMP Deviations: manufactured under the same conditions as those found to be subpotent.
Class IIFDA: TerminatedRLC Labs Inc.
DrugSep 23, 2020
RLC Labs Nature-Throid, Thyroid USP [liothyronine (T3) 4.5 mcg and levothyroxine (T4) 19 recall — FDA D-1598-2020
CGMP Deviations: manufactured under the same conditions as those found to be subpotent.
Class IIFDA: TerminatedRLC Labs Inc.
DrugSep 23, 2020
RLC Labs Nature-Throid, Thyroid USP [liothyronine (T3) 6.75 mcg and levothyroxine (T4) 28.5 recall — FDA D-1597-2020
CGMP Deviations: manufactured under the same conditions as those found to be subpotent.
Class IIFDA: TerminatedRLC Labs Inc.
DrugSep 23, 2020
RLC Labs Nature-Throid, Thyroid USP [liothyronine (T3) 11.25 mcg and levothyroxine (T4) 47.5 recall — FDA D-1599-2020
CGMP Deviations: manufactured under the same conditions as those found to be subpotent.
Class IIFDA: TerminatedRLC Labs Inc.
DrugSep 23, 2020
RLC Labs Nature-Throid, Thyroid USP [liothyronine (T3) 15.75 mcg and levothyroxine (T4) 66.5 recall — FDA D-1601-2020
CGMP Deviations: manufactured under the same conditions as those found to be subpotent.
Class IIFDA: TerminatedRLC Labs Inc.
DrugSep 23, 2020
RLC Labs WP Thyroid, Westhroid Pure, 1 Grain (65 mg) Thyroid USP recall — FDA D-1609-2020
CGMP Deviations: manufactured under the same conditions as those found to be subpotent.
Class IIFDA: TerminatedRLC Labs Inc.
DrugSep 23, 2020
Real Clean Distribuciones SA de CV scent theory KEEP CLEAN Moisturizing Hand Sanitizer, 70% recall — FDA D-1580-2020
CGMP Deviations: Born Basic Anti Bac was found to be below the label claim for ethanol content and contained methanol. Other products were recalled because they were manufactured in the…
Class IIFDA: TerminatedReal Clean Distribuciones SA de CV
VehicleSep 23, 2020
Tiguan LWB seat belts recall — NHTSA campaign 20V579000
Volkswagen Group of America, Inc. (Volkswagen) is recalling certain 2020 Tiguan LWB vehicles. The third row seat belt anchor bolts may not have been properly torqued.
seat beltsVolkswagen Group of America, Inc.
VehicleSep 23, 2020
Mustang pedals and linkages recall — NHTSA campaign 20V573000
Ford Motor Company (Ford) is recalling certain 2020 Mustang vehicles equipped with automatic transmissions. The brake pedal bracket may fracture during sudden stopping.
pedals and linkagesFord Motor Company
VehicleSep 23, 2020
Ford camera recall — NHTSA campaign 20V575000
Ford Motor Company (Ford) is recalling certain 2020 Ford F-150, F-250, F-350, F-450, F-550, Explorer, Mustang, Transit, Expedition, Escape, Ranger and Edge, and Lincoln Nautilus and Corsair…
cameraFord Motor Company
VehicleSep 22, 2020
Nissan glass, side/rear recall — NHTSA campaign 20V570000
Nissan North America, Inc. (Nissan) is recalling certain 2020 Altima, Maxima and Leaf vehicles. The rear window glass may not remain properly secured to the vehicle.
glass, side/rearNissan North America, Inc.
Medical DeviceSep 16, 2020
Merge PACS recall — FDA Z-2944-2020
Measurements done on the Merge PACS generated MPR s may have incorrect measurements.
Class IIFDA: TerminatedMerge Healthcare, Inc.
Medical DeviceSep 16, 2020
Intuitive Surgical ION Reprocessing Accessories Kit, IF1000 (Part Number: 490024-03) recall — FDA Z-2950-2020
One type of the ION Catheter Reprocessing Covers (PN 490114-02) has the potential to become disengaged or incorrectly engaged to the ION Fully Articulating Catheter which can result in…
Class IIFDA: OngoingIntuitive Surgical, Inc.
Medical DeviceSep 16, 2020
Smiths Medical ASD Bivona Mid-Range Aire-Cuf Adult Tracheostomy Tube This tube is intended recall — FDA Z-2946-2020
Label has the incorrect size for the tracheotomy tube.
Class IIFDA: TerminatedSmiths Medical ASD Inc.
Medical DeviceSep 16, 2020
CareFusion 303 PC Unit Front Case with Keypad Replacement Kits: TC10008389 ASSY CASE FRONT recall — FDA Z-2910-2020
The pump module keypad may exhibit keys that are unresponsive or stuck as a result of fluid ingress potentially resulting in a delay to the start of infusion, interruption of infusion, or…
Class IFDA: OngoingCareFusion 303, Inc.
Medical DeviceSep 16, 2020
Medical Components, Inc dba MedComp Medcomp 15.SF X 24CM Titan HD CATHETER recall — FDA Z-2940-2020
Kits were packaged with the incorrect size valve peelable introducer. The kits include a 15F instead of the correct 16F valve peelable introducer
Class IIFDA: TerminatedMedical Components, Inc dba MedComp
Medical DeviceSep 16, 2020
Intuitive Surgical Ion Catheter Reprocessing Cover, IF1000 (Part Number:490114-02) recall — FDA Z-2949-2020
One type of the ION Catheter Reprocessing Covers (PN 490114-02) has the potential to become disengaged or incorrectly engaged to the ION Fully Articulating Catheter which can result in…
Class IIFDA: OngoingIntuitive Surgical, Inc.
Medical DeviceSep 16, 2020
Qiagen Sciences QIAstat-Dx Respiratory SARS-CoV-2 Panel REF 691223 (US IVD under FDA EUA) recall — FDA Z-2938-2020
There is an increased rate of potential false positive results for the Influenza A (no subtype) target, which may lead to 1) inappropriate antiviral use, 2) erroneous or delayed…
Class IIFDA: TerminatedQiagen Sciences LLC
Medical DeviceSep 16, 2020
CareFusion 303 BD Alaris System; Alaris Syringe Module Model 8110; BD Alaris System; Alaris recall — FDA Z-2882-2020
The Alaris PC unit can display incorrect syringe type and/or syringe sizes. This could result in delays in infusion, under-infusion, or over-infusion.
Class IFDA: OngoingCareFusion 303, Inc.
Medical DeviceSep 16, 2020
Talladium Luminesse Zirconia Discs, Zirconia HT Disc 98x20mm A1, Shaded Zirconia Blend 2.0 recall — FDA Z-2943-2020
The linear shrinkage on the zirconia blank disc s part label is incorrect. The average linear shrinkage found on the product label was outside the acceptable range. The acceptable average…
Class IIFDA: TerminatedTalladium Inc.
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Recent recall archives
Browse recent months with enough recall history for useful comparison.
October 2026179 records · 4 categoriesSeptember 2026363 records · 4 categoriesAugust 2026302 records · 4 categoriesJuly 2026370 records · 4 categoriesJune 2026376 records · 4 categoriesMay 2026340 records · 4 categoriesApril 2026415 records · 4 categoriesMarch 2026190 records · 4 categoriesFebruary 2026331 records · 4 categoriesJanuary 2026212 records · 4 categoriesDecember 2025389 records · 4 categoriesNovember 2025326 records · 4 categories