Kingdom Creamery of Vermont LLC Recalls

Product may be contaminated Listeria monocytogenes.

FDAJul 29, 2022ME, MA, VT• Kingdom Creamery of Vermont LLC

Sorbet Base Mix (Kingdom Creamery) – Listeria contamination (2022)

Product may be contaminated Listeria monocytogenes.

FDAJul 29, 2022ME, MA, VT• Kingdom Creamery of Vermont LLC

Rococo Ice Cream Base Mix (Kingdom Creamery) – Listeria risk (2022)

Product may be contaminated Listeria monocytogenes.

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Class IHigh

FDAJul 29, 2022ME, MA, VT• Kingdom Creamery of Vermont LLC

Chocolate Soft Serve Mix (Kingdom Creamery) – Listeria risk (2022)

Product may be contaminated Listeria monocytogenes.

FDAJul 29, 2022ME, MA, VT• Kingdom Creamery of Vermont LLC

SOCO Creamery Base Mix (Kingdom Creamery) – Listeria contamination (2022)

Product may be contaminated Listeria monocytogenes.

FDAJul 29, 2022ME, MA, VT• Kingdom Creamery of Vermont LLC

Underwater Communication Devices (Ocean Technology) – fire hazard (2022)

Fire/Burn Risk

This recall involves the PowerCom 3000D, 5000D and MilCom 6000D underwater communication devices sold with the RBLi-4 Lithium battery pack and the batteries that are also sold separately. The PowerCom, MilCom and RBLi-4 products are used in all SCUBA diving. The recalled RBLi-4 battery packs are in a waterproof housing and supply power to the PowerCom and MilCom products. PowerCom and MilCom along with the model numbers are printed on the front of the underwater communication devices.

CPSCJul 28, 2022Nationwide• Undersea Systems International Inc., dba Ocean Technology Systems, of Santa Ana, California

Evaporator Coil Drain Pans (Daikin) – expanded product recall (2022)

Fire/Burn Risk

This recall expands the scope of a previous recall that involved certain evaporator coil drain pans installed with condensing gas furnaces in an up-flow coil configuration. The recall now also includes those drain pans installed with certain configurations of competitor branded (not Goodman, Daikin or Amana-branded) non-condensing residential gas furnaces in a vertical, or "up-flow," coil configuration, as shown in the table below: Type Coil Configuration Affected Furnace Brands Affected Coil Serial Numbers Dates Sold Condensing furnace system Up-Flow (Coil above Furnace) All Prefixes ranging from 1901 through 2101 Jan. 2019 through Nov. 2021 Non-condensing furnace system (Certain configurations) Up-Flow (Coil above Furnace) Any "competitor" brand (excludes Goodman, Daikin or Amana branded furnaces) Prefixes ranging from 1901 through 2101 Jan. 2019 through Nov. 2021 NOTE: Furnace systems that were repaired with a new evaporator coil drain pan between January 2019 and November 2021, with the serial number range listed above, are also included in this recall. Whether a non-condensing furnace system falls within the scope of the expanded recall depends on the location of the burners, which, if unknown, can be verified through DCT's model verification tool at: https://www.recallrtr.com/drainpan. Affected units can be identified through serial numbers found on the evaporator coil or the case, which sits atop the vertically installed furnace. The furnace brand and model number can be found on the furnace on the "Energy Guide" label. Consumers can refer to the instructions on DCT's model verification tool at: https://www.recallrtr.com/drainpan. The model number of the outdoor condenser may also be required and can be found on a label attached to the product.

CPSCJul 28, 2022Nationwide• Daikin Comfort Technologies Manufacturing, L.P. (formerly Goodman Manufacturing Company, L.P.) of Houston, Texas

Aesop Post-Poo Drops (Emeis Cosmetics) – child safety risk (2022)

Fire/Burn Risk

This recall involves Aesop Post-Poo Drops, a bathroom deodorizer in a 100 mL amber glass bottle, with a continuous thread pipette dispenser closure. The bottle has a black and cream label with the brand name Aesop. The UPC number 9319944009200 is located on the rear of the bottle, directly below the ingredients list. The deodorizer product was also sold in four versions of the Home Kit: The Protector, The Seasoned Wayfarer, The Melodist, and The Familiar Horizon. The UPC numbers for four versions of the Home Kit are located on the rear of the printed sleeve. Only the Aesop Post-Poo Drops in the kit are included in this recall. The product names and UPC are as follows: Product Name UPC Description Post-Poo Drops 9319944009200 100 mL amber glass bottle, with a continuous thread pipette dispenser closure The Protector 9319944030198 100 mL amber glass bottle, with a continuous thread pipette dispenser closure The Seasoned Wayfarer 9319944023794 100 mL amber glass bottle, with a continuous thread pipette dispenser closure The Melodist 9319944022278 100 mL amber glass bottle, with a continuous thread pipette dispenser closure The Familiar Horizon 9319944016017 100 mL amber glass bottle, with a continuous thread pipette dispenser closure. This recall also involves four Aesop Oil Burner Blends: Anouk, Beatrice, Catherine, and Isabelle. The aromatic oil blends intended to be used in an oil burner. These products include a black and cream label with the brand name Aesop and the blend name. They come in a 25 mL amber glass bottle with a continuous thread closure and flow restrictor insert. The UPC numbers for the Oil Burner Blends are located on the rear of each bottle, below the ingredients lists. The product names and UPC for the recalled Oil Burner Blend products are as follows: Product Name UPC Description Anouk Oil Burner Blend 9319944000696 25 mL amber glass bottle with a continuous thread closure and flow restrictor insert Beatrice Oil Burner Blend 9319944000702 25 mL amber glass bottle with a continuous thread closure and flow restrictor insert Catherine Oil Burner Blend 9319944000689 25 mL amber glass bottle with a continuous thread closure and flow restrictor insert Isabelle Oil Burner Blend 9319944016871 25 mL amber glass bottle with a continuous thread closure and flow restrictor insert

CPSCJul 28, 2022Nationwide• Emeis Cosmetics Pty Ltd., of Collingwood, Victoria, Australia

Cummins L9 Engine (Cummins) – Engine Control Module (2022)

Cummins, Inc. (Cummins) is recalling certain X15, X12, L9, and B6.7 diesel engines. The engine control module (ECM) may experience an internal electrical short-circuit, causing the engine to stall.

NHTSAJul 28, 2022Nationwide• CUMMINS

Orca Foam Cube (Gelita Medical) – Endotoxin Levels (2022)

In routine bioburden testing, higher than acceptable levels of Endotoxins were observed.

FDAJul 27, 2022Nationwide• GELITA MEDICAL GMBH Uferstr. 7 Eberbach Germany

Vanta Clinician Programmer (Medtronic) – Communication Issue (2022)

Potential communication issue in which the Vanta Clinician Programmer Application (CP App) A71200 v2.0.2455 may be unable to connect with a Vanta Implantable Neurostimulator (INS) Model 977006 when a patient is implanted with more than one neurostimulator.

FDAJul 26, 2022AL, AK, AZ +47 more• Medtronic Neuromodulation

Vanta Clinician Programmer (Medtronic) – Error Code Issue (2022)

Potential for Vanta Clinician Programmer Application (CP App) A71200 v2.0.2455 to display an Unexpected Device Error Code 1502 Message, and the user will be unable to perform programming of the Vanta Implantable Neurostimulator (INS) Model 977006.

FDAJul 26, 2022Nationwide• Medtronic Neuromodulation

Nobel Biocare N1 Implant (Nobel Biocare) – Aspiration Risk (2022)

Due to the presence of a burr which may cause an aspiration risk to patient during surgical procedure.

FDAJul 25, 2022Nationwide• Nobel Biocare Vastra Hamngatan 1 Goteborg Sweden

HLS Set Advanced (Maquet) – Sterility Barrier (2022)

The firm has expanded the recall for the HLS Set Advanced regarding a potential breach in the sterility barrier that may result in compromised product sterility (prior recall was initiated November 6, 2020).

FDAJul 22, 2022Nationwide• Maquet Medical Systems USA

Corin MetaFix Hip Stem (Corin) – Incorrect Labeling (2022)

One MetaFix size 7 collarless stem from batch 478179 which was incorrectly labelled as a MetaFix size 3 collared stem from batch 485630.

Low

FDAJul 22, 2022Nationwide• Corin Ltd Unit 1-57-8 Corinium Centre Cirencester United Kingdom

HLS Set Advanced (Maquet) – Sterility Barrier (2022)

FDAJul 22, 2022Nationwide• Maquet Medical Systems USA

Autosoft 90 Cannula (Unomedical) – Insulin Fill Value (2022)

The IFU incorrectly states the insulin fill value of two sizes of cannula which can result in an initial insulin infusion to be fewer units than intended.

Low

FDAJul 21, 2022CA• Unomedical A/S Aaholmvej

LiftActiv Peptide-C Ampoules (Vichy Laboratoires) – Laceration Risk (2022)

Laceration Risk

This recall involves Liftactiv Peptide-C Ampoules 1.8ml (10 pack) and Liftactiv Peptide-C Ampoules 1.8ml (30 pack) which are facial serums. The serum is packaged in amber-colored glass ampoules with the following batch numbers: 54T61Q, 54T91Q, 54TD1Q, 54TD2Q, 54TN1Q, 54TN2Q, 54TN3Q, 54TO1Q, 54U11Q, 54U12Q, 54U21Q, 54U31Q, 54U32Q, 54U41S, 54U42S, 54U51S, 54U52S, 54U53S, 54U54S, 54U61S, 54U72S, 54U91S, 54U62S, 54U92S, 54UD1S, 54UO1S, 54W11S, 54W12S, 54W13S, 54W21S. The batch number is printed on the bottom or side of the pack.