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The Newark Nut Store

The Newark Nut Store Recalls

All product recalls associated with The Newark Nut Store.

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Recall Summary

Total Recalls

1000

Past Year

Class I (Serious)

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 1101–1120 of 2670 recalls

Dark Chocolate Gummy Bears (Newark Nut Store) – Packaging Concern (2019)

Kopper s Chocolate has initiated recall of Koppers Chocolate Dark Chocolate Gummy Bears, 4oz (113g) retail package, metallized foil resealable pouch, 12 pouches per case, printed BB: 08/2020 because the product packaging only identifies soy as an allergen. The product does not list milk , which is an allergen .

Class IIModerate

FDASep 25, 2019NJ, NY, PA• The Newark Nut Store

Randox Laboratories, Limited Ardmore; 55 The Diamond Road Crumlin United Kingdom: RANDOX NEFA (Non-Esterified Fatty Acids) FA115 Lot 485343...

Non-Esterified Fatty Acids (NEFA) FA115 batch 485343 is not meeting the performance claims and should not be used in any further testing.

FDASep 23, 2019WV• Randox Laboratories, Limited Ardmore; 55 The Diamond Road Crumlin United Kingdom

Losartan Potassium Tablets 50mg (Torrent) – NMBA Impurity (2019)

CGMP Deviations: FDA lab confirmed presence of an impurity, N-Methylnitrosobutyric acid (NMBA) in the finished product above the interim acceptable daily intake level of 9.82 parts per million.

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Class IIModerate

FDASep 19, 2019Nationwide• Torrent Pharma Inc.

Losartan/Hydrochlorothiazide Tablets 100mg (Torrent) – NMBA Impurity (2019)

CGMP Deviations: FDA lab confirmed presence of an impurity, N-Methylnitrosobutyric acid (NMBA) in the finished product above the interim acceptable daily intake level of 9.82 parts per million.

Class IIModerate

FDASep 19, 2019Nationwide• Torrent Pharma Inc.

Losartan/Hydrochlorothiazide Tablets 50mg (Torrent) – NMBA Impurity (2019)

CGMP Deviations: FDA lab confirmed presence of an impurity, N-Methylnitrosobutyric acid (NMBA) in the finished product above the interim acceptable daily intake level of 9.82 parts per million.

Class IIModerate

FDASep 19, 2019Nationwide• Torrent Pharma Inc.

Losartan Potassium Tablets 100mg (Torrent) – NMBA Impurity (2019)

CGMP Deviations: FDA lab confirmed presence of an impurity, N-Methylnitrosobutyric acid (NMBA) in the finished product above the interim acceptable daily intake level of 9.82 parts per million.

Class IIModerate

FDASep 19, 2019Nationwide• Torrent Pharma Inc.

Infant's Gas Relief Drops (GCP) – Microbial Contamination (2019)

Microbial Contamination of Non-Sterile Product.

Class IIModerate

FDASep 18, 2019Nationwide• GCP Laboratories Inc

Povidone Iodine Ophthalmic Solution (Avella) – Sterility Risk (2019)

Lack of sterility assurance.

Class IIModerate

FDASep 18, 2019Nationwide• Avella of Deer Valley, Inc. Store 38

Abbott Calcilo XD Infant Formula (Abbott) – seal defect (2019)

Off color and odor. Compromised can seam due to product (powder) in the seam, this poor seal potentially allowed air into the container.

Class IIModerate

FDASep 13, 2019Nationwide• Abbott Laboratories

Fentanyl Citrate (Spectrum) – glass contamination (2019)

CGMP Deviations: Received notice from supplier that there is potential glass contamination.

Class IIModerate

FDASep 12, 2019CA, CO, IN +2 more• Spectrum Laboratory Products

Stormrider Air Rifle (DIANA) – Discharge risk (2019)

This recall involves the DIANA Stormrider Gen 2 Air Rifle with 2-stage adjustable trigger. The recalled products are .177 and .22 caliber, pre-charged pneumatic air rifles that are powered by a compressed air cylinder. "DIANA Stormrider" as well as the caliber and serial number are printed on each affected air rifle. Air rifles with the following item and serial numbers are included in the recall: Recalled DIANA Stormrider Gen 2 Air Rifles Item Numbers 1900001 & 1900101 Serial Numbers 2318220145032949E - 2318229955034368E 2318229955075924I - 2318229955076323I

CPSCSep 10, 2019Nationwide• Shaoxing Snowpeak Air Gun Factory, of China

Anagrelide Capsules (Torrent) - impurity specification (2019)

Failed Impurities/Degradation Specifications: High Out Of Specification results for impurities detected during routine stability testing.

Class IIModerate

FDASep 6, 2019Nationwide• Torrent Pharma Inc.

Teryx Recreational Vehicles (Kawasaki) - Crash and Injury Risks (2019)

This recall involves model year 2019 and 2020 Teryx and Teryx4 recreational off-highway vehicles (ROVs), models KRF800FKF/L, KRF800GKF/A/AL/L, KRF800HKF/L, KRT800FKF/L, KRT800GKF/A/AL/L, KRT800HKF/L, KRF800FLF/L, KRF800GLF/L, KRF800HLF/L, KRT800FLF/L, KRT800GLF/A/AL/L and KRT800HLF/L. The recalled vehicles were sold in various colors including: black, camo, gray, green, orange and white; and in three different styles: Non-EPS, EPS and EPS LE. The vehicles have either two or four seats, automotive style controls and a rear box. Kawasaki is printed on the vehicle's hood and rear box. Teryx or Teryx4 is printed on the right and left front fender.

CPSCSep 4, 2019Nationwide• Kawasaki Motors Manufacturing Corp. U.S.A., Lincoln, Neb.

Golf Cars (Yamaha) – Fire Risk (2019)

Fire/Burn Risk

This recall involves the following model year 2017 through 2019 golf cars, personal transportation and specialty vehicles and utility vehicles. The vehicles were sold in various colors including blue, green, red, white, tan and silver. The model and serial number can be found on a label under the seat or cargo bed on the left or right side. Model Year Model Name Model Prefix Serial Number Range 2017 Drive2 Fleet DC (J0C1) J0C 0000103 0011333 Drive2 Fleet AC (J0J1) J0J 0000103 0002000 Adventurer Two AC (JW33) JW3 0200166 0200213 2018 Drive2 Fleet DC (J0C2) J0C 0100112 0111700 Drive2 Fleet AC (J0J2) J0J 0100110 0102099 Adventurer Two AC (JW34) JW3 0300166 0300214 2019 Drive2 Fleet DC (J0C3) J0C 0200101 0210200 UMAX TWO AC (J0H1) J0H 0000145 0000493 UMAX Rally AC (J0N1) J0N 0000116 0000147 UMAX Rally 2+2 AC (J0R1) J0R 0000101 0000180

CPSCAug 28, 2019Nationwide• Yamaha Motor Manufacturing Corporation of America, of Newnan, Ga.

Karl Storz Endoscopy: Karl Storz, Model # 11161C2, Flexible Neuroscope

During a complaint investigation it was determined that an error was observed within the instruction manual included with some scopes. Specifically, The Quick Connector Kits (QCK) and tray information, specified for the STERIS System 1E (SS1E) sterilization method within the instruction manual is incorrect. If the user uses SS1E to sterilize the impacted scopes and referred to the manual concerning the QCK information, the sterility of reprocessed scope cannot be guaranteed.

FDAAug 27, 2019AL, AZ, CA +25 more• Karl Storz Endoscopy

Karl Storz Endoscopy: Karl Storz RHINO-LARYNGO-BRONCHO FIBERSCOPE, Model # 110...

FDAAug 27, 2019AL, AZ, CA +25 more• Karl Storz Endoscopy

Karl Storz Endoscopy: Karl Storz NEURO-FIBERSCOPE, Model # 11282BN1, Flexible P...

FDAAug 27, 2019AL, AZ, CA +25 more• Karl Storz Endoscopy

2020 THOR MOTOR COACH MAJESTIC Recall: ELECTRICAL SYSTEM:12V/24V/48V BATTERY:CABLES

Fire/Burn Risk

Thor Motor Coach (TMC) is recalling certain 2020 Chateau, Daybreak, Four Winds, Freedom Elite, Majestic, Outlaw and Quantum motorhomes. The battery cables may loosen on the battery isolation manager (BIM) or battery isolation relay (BIR), causing premature BIN/BIR failure or electrical arcing.

NHTSAAug 20, 2019Nationwide• THOR MOTOR COACH

RESPIRATORY THERAPEUTICS GROUP LLC: RespVent Closed Suction System T-Piece Tracheostomy Adult...

It has been determined that some units of catheters were not tightly connected to the thumb port. This may result in the catheter disconnecting from the thumb port which could reduce the suction performance and make it difficult to remove from the patient's trachea.

FDAAug 19, 2019Nationwide• RESPIRATORY THERAPEUTICS GROUP LLC

Similac Pro-Sensitive (Abbott) – packaging mix-up (2019)

a limited number of Similac Pro-Advance 2oz. Ready to Feed (RTF) bottles from a single batch were packaged in Similac Pro-Sensitive cartons.

Class IIModerate

FDAAug 16, 2019AL, IN, IA +6 more• Abbott Nutrition, Division of Abbott Laboratories