Safety Recalls
RSS ↗17,560 recalls across FDA food, drug, and medical device recalls, CPSC consumer products, and NHTSA vehicles.
Showing 5,601–5,650 of 17,560
- Class II
Drug Recall · October 7, 2025
Prazosin Hydrochloride, Capsules, USP, 1 mg, Rx only, Distributed by TEVA PHARMACEUTICALS USA, INC., North Wales, PA 19454, a) 100 Capsules, NDC 0093-4067-01, b) 1000 Capsules, NDC 0093-4067-10CGMP Deviations-Test results for N-nitroso Prazosin impurity C that are above the Carcinogenic Potency Categorization Approach (CPCA) acceptable intake limit for the above specified lots.
- Unclassified
Vehicle Recall · October 7, 2025
2023 LUCID AIR, 2024 LUCID AIR, 2025 LUCID AIRA rearview image that does not appear or fails to accurately depict behind the vehicle increases the risk of a crash.
- Unclassified
Vehicle Recall · October 7, 2025
Toyota Motor Engineering & Manufacturing
2025 TOYOTA SIENNA HYBRIDImproperly welded seat rails can prevent the seat from adequately restraining an occupant during a crash, increasing the risk of injury.
- Class II
Medical Device Recall · October 7, 2025
Meridian Bioscience, alethia c. Difficile, Catalog Number 480050, Nucleic Acid Amplification Test AssayThe cap on the reaction buffer tube may be missing the black rubber gasket resulting in the potential for leakage and reduced buffer volume.
- Class II
Drug Recall · October 7, 2025
Prazosin Hydrochloride, Capsules, USP, 5 mg, Rx only, Distributed by TEVA PHARMACEUTICALS USA, INC., North Wales, PA 19454, a) 100 Capsules, NDC 0093-4069-01, b) 250 Capsules, NDC 0093-4069-52, c) 500CGMP Deviations-Test results for N-nitroso Prazosin impurity C that are above the Carcinogenic Potency Categorization Approach (CPCA) acceptable intake limit for the above specified lots.
- Class II
Medical Device Recall · October 7, 2025
GM85 Digital Mobile X-ray imaging System; Model Number: GM85;The four (4) M5 bolts that secure the Tube Head Unit to the end of the arm may loosen or fracture due to metal fatigue.
- Class II
Medical Device Recall · October 7, 2025
SimplyGo Mini, Standard Battery Kit; Product code: 1116816; The affected battery kits are sold as accessories for the SimplyGo Mini: SimplyGo Mini Portable Oxygen Concentrator Product code: 1113Certain serial numbers of the SimplyGo Mini standard battery kit contain a defective chip which can lead the battery to either fail to charge or lose voltage output when in use in the device. If the fault occurs while the device is running on battery power, the SimplyGo Mini will shut down and stop providing oxygen to the user. This may happen at a temperature within the specified operating temperature range of the SimplyGo Mini.
- Unclassified
Vehicle Recall · October 7, 2025
2024 LUCID AIR, 2025 LUCID AIRA disconnected half shaft can result in a loss of drive power, increasing the risk of a crash.
- Class II
Drug Recall · October 7, 2025
Carbidopa, Levodopa, Entacapone Tablets, 25 mg/100 mg/200 mg, 100-count bottle, Rx Only, Manufactured for: Rising Pharma Holdings, Inc. East Brunswick, NJ, 08816, Manufactured by Suven PharmaceuticalsProduct mix up: complaint received that sealed medication bottle contained Carbidopa, Levodopa, and Entacapone film-coated tablets (37.5 mg/150 mg/200 mg) instead of labelled lower strength Carbidopa, Levodopa, and Entacapone film-coated tablets (25 mg/100 mg/200 mg).
- Class II
Medical Device Recall · October 7, 2025
Meridian Bioscience, Group B Streptococcus, Catalog Number 480050, Nucleic Acid Amplification Test AssayThe cap on the reaction buffer tube may be missing the black rubber gasket resulting in the potential for leakage and reduced buffer volume.
- Class II
Medical Device Recall · October 7, 2025
Good Neighbor Pharmacy, TRUE METRIX Self Monitoring Blood Glucose Meter. Model/Catalog Number: RE4011-01.Manufacturing defect causing LCD display issues with missing or partial segments (ghosting) that can result in misreading glucose values, potentially leading to inappropriate treatment decisions for diabetes management.
- Class II
Drug Recall · October 7, 2025
Prazosin Hydrochloride, Capsules, USP, 2 mg, Rx only, Distributed by TEVA PHARMACEUTICALS USA, INC., North Wales, PA 19454, a) 100 Capsules, NDC 0093-4068-01, b) 1000 Capsules, NDC 0093-4068-10CGMP Deviations-Test results for N-nitroso Prazosin impurity C that are above the Carcinogenic Potency Categorization Approach (CPCA) acceptable intake limit for the above specified lots.
- Class II
Food Recall · October 7, 2025
Loaded Veggie Grain Bowl; NET WT. 10/90 OZ (309g) NO UPC Identifying N4L code: V3FRPotential contamination with Listeria monocytogenes.
- Class II
Food Recall · October 7, 2025
Eagle Spice and Extract Co., Inc.
Eagle Spice Ground Ginger 16 oz.Contains elevated levels of lead (Pb)
- Class II
Food Recall · October 7, 2025
Loaded Veggie Grain Bowl; Net Wt. 10.90 Oz (309g) GTIN code: 00818905028162Potential contamination with Listeria monocytogenes
- Class I
Food Recall · October 7, 2025
" Product Name: Pastured Grade AA Large Eggs " Product Description: Egg Carton, 12 eggs per dozen " Pack/Julian Date(s): Julian date 241(Aug 30) to 244 (Sep 2) and 246 (Sep 4) to 247 (Sep 5), Best byEggs may be contaminated with Salmonella.
- Class II
Medical Device Recall · October 6, 2025
Siemens Healthcare Diagnostics, Inc.
3gAllergy Specific IgE Universal Kit; Kit Component: 3gAllergy Specific IgE Adjustor Antibody (L2UNS1), 3gAllergy Specific IgE Control Antibody (L2UNS2); Siemens Material Number (SMN): 10380875; CaThe barcode orientation on affected devices causes incorrect scanning order of tubes within the allergen holder wedge. When using an IMMULITE 2000 / IMMULITE 2000 XPi instrument in combination with a Zebra barcode scanner, the instrument will not correctly recognize the position of tubes within the allergen holder wedge.
- Class III
Medical Device Recall · October 6, 2025
POLYMEDCO, INC. / POLYMEDCO CANCER DIAGNOSTIC PRODUCTS, LLC
OC-Auto FOBT-CHEK Negative Controls is the negative hemoglobin control materials designed to monitor FOBT (Fecal Occult Blood Test)A labeling error was identified on the affected product. The expiration date on the kit box label and on the vial labels incorrectly stated the expiration date as 2026-01-16. The correct expiration date should be 2027-01-17.
- Class II
Medical Device Recall · October 6, 2025
Siemens Healthcare Diagnostics, Inc.
IMMULITE 2000 Oak Mix Specific Allergen; Siemens Material Number (SMN): 10386105; Catalog Number: L2KUN6;The barcode orientation on affected devices causes incorrect scanning order of tubes within the allergen holder wedge. When using an IMMULITE 2000 / IMMULITE 2000 XPi instrument in combination with a Zebra barcode scanner, the instrument will not correctly recognize the position of tubes within the allergen holder wedge.
- Class II
Drug Recall · October 6, 2025
Desipramine Hydrochloride Tablets, USP, 50 mg, 100 count bottle (NDC 23155-580-01), Rx only, Manufactured by: USV Private Limited, Daman, India, Manufactured for: Avet Pharmaceuticals Inc., East BrunsCGMP Deviations: N-Nitroso Desipramine impurity exceeding the permissible acceptable daily intake level.
- Class II
Medical Device Recall · October 6, 2025
Olympus Corporation of the Americas
Brand Name: Olympus Single Use Electrosurgical Snare SD-400 Product Name: Single Use Electrosurgical Snare Model/Catalog Number: SD-400U-10 Product Description: These instruments have been designedSterility compromised from small holes that may occur during packaging of the device pouches into the shelf carton and/or during transportation of the shelf carton.
- Class II
Drug Recall · October 6, 2025
Desipramine Hydrochloride Tablets, USP, 10 mg, 100 - count bottle (NDC 23155-578-01), Rx only, Manufactured by: USV Private Limited, Daman, India, Manufactured for: Avet Pharmaceuticals Inc., East BruCGMP Deviations: N-Nitroso Desipramine impurity exceeding the permissible acceptable daily intake level.
- Class II
Medical Device Recall · October 6, 2025
Applied Medical Technology Inc
Applied Medical Technology, Inc., NutraGlide, 6 F- 8 F x 90 Nasal Feeding Tube with Stylet and ENfit, REF NFT-06090-IThe nasal feeding tube may be occluded
- Unclassified
Vehicle Recall · October 6, 2025
2023 MACK GRANITE (GR), 2023 MACK MD, 2024 MACK ANTHEM (AN), 2024 MACK MD, 2025 MACK GRANITE (GR), 2025 MACK MDAn improperly welded seat belt anchorage bracket can detach during a crash, increasing the risk of injury.
- Class II
Drug Recall · October 6, 2025
Desipramine Hydrochloride Tablets, USP, 25 mg, 100 count bottle (NDC 23155-579-01), Rx only, Manufactured by: USV Private Limited, Daman, India, Manufactured for: Avet Pharmaceuticals Inc., East BrunsCGMP Deviations: N-Nitroso Desipramine impurity exceeding the permissible acceptable daily intake level.
- Class II
Medical Device Recall · October 6, 2025
Applied Medical Technology Inc
Applied Medical Technology, Inc., NutraGlide, 6 F- 8 F x 55 Nasal Feeding Tube with Stylet and ENfit, REF NFT-06055-IThe nasal feeding tube may be occluded
- Class II
Medical Device Recall · October 6, 2025
Applied Medical Technology Inc
Applied Medical Technology, Inc., NutraGlide, 5 F- 6 F x 90 Nasal Feeding Tube with Stylet and ENfit, REF NFT-05090-IThe nasal feeding tube may be occluded
- Class I
Medical Device Recall · October 6, 2025
Tandem Mobi Insulin Pump: Description/Catalog: Tandem insulin pumps are battery-operated infusion pumps capable of both basal and bolus delivery of insulin. The pumps utilize a motor-driven mechanismInsulin pump includes a vibration motor that gives tactile feedback for any alerts, alarms, or malfunctions. Pump may exhibit false vibration motor failure due to a software issue causing Malfunction 12: "Pump cannot operate, the mobile app can no longer receive data from the pump. Insulin delivery and any active CGM Sessions have been stopped", which could result in hyperglycemia.
- Class II
Medical Device Recall · October 6, 2025
Applied Medical Technology Inc
Applied Medical Technology, Inc., NutraGlide, 5 F- 6 F x 55 Nasal Feeding Tube with Stylet and ENfit, REF NFT-05055-N-IThe nasal feeding tube may be occluded
- Class II
Medical Device Recall · October 6, 2025
Olympus Corporation of the Americas
Brand Name: Olympus Single Use Single Use Electrosurgical Snare SD-400 Product Name: Single Use Single Use Electrosurgical Snare Model/Catalog Number: SD-U400U-15 Product Description: These instrumSterility compromised from small holes that may occur during packaging of the device pouches into the shelf carton and/or during transportation of the shelf carton.
- Class II
Medical Device Recall · October 6, 2025
Applied Medical Technology Inc
Applied Medical Technology, Inc., NutraGlide, 5 f - 6F x 55 Nasal Feeding Tube with Stylet and ENfit, REF NFT-05055-IThe nasal feeding tube may be occluded
- Class II
Medical Device Recall · October 6, 2025
Siemens Healthcare Diagnostics, Inc.
Food Panel 3 Specific Allergen; Siemens Material Number (SMN): 10385891; Catalog Number: FP3L4;The barcode orientation on affected devices causes incorrect scanning order of tubes within the allergen holder wedge. When using an IMMULITE 2000 / IMMULITE 2000 XPi instrument in combination with a Zebra barcode scanner, the instrument will not correctly recognize the position of tubes within the allergen holder wedge.
- Class II
Medical Device Recall · October 6, 2025
Eterna SCS IPG (Implantable Pulse Generator), Model Number 32400There is a potential issue affecting Eterna Spinal Cord Stimulation (SCS) Implantable Pulse Generators (IPGs), Model 32400 and Liberta RC Deep Brain Stimulation (DBS) Implantable Pulse Generators (IPGs), Model 62400 . These devicess may experience a loss of communication with the Clinician Programmer (CP) and/or the Patient Controller (PC).
- Unclassified
Vehicle Recall · October 6, 2025
2024 RAM PROMASTER, 2025 RAM PROMASTERA loss of drive power increases the risk of a crash.
- Class II
Drug Recall · October 6, 2025
Desipramine Hydrochloride Tablets, USP, 100 mg, 100 count bottle (NDC 23155-582-01), Rx only, Manufactured by: USV Private Limited, Daman, India, Manufactured for: Avet Pharmaceuticals Inc., East BrunCGMP Deviations: N-Nitroso Desipramine impurity exceeding the permissible acceptable daily intake level.
- Class II
Food Recall · October 6, 2025
Frozen Organic Spinach Net Wt. 10 oz (283.5g) poly bags packaged under the following brands: 1. Sno Pac Frozen Vegetables, UPC 0 24284-96910 5. Keep Frozen. Packed and Distributed by: Sno PacOrganic Spinach has the potential to be contaminated with Listeria monocytogenes.
- Class II
Drug Recall · October 6, 2025
Desipramine Hydrochloride Tablets, USP, 75 mg, 100 count bottle (NDC 23155-581-01), Rx only, Manufactured by: USV Private Limited, Daman, India, Manufactured for: Avet Pharmaceuticals Inc., East BrunsCGMP Deviations: N-Nitroso Desipramine impurity exceeding the permissible acceptable daily intake level.
- Class II
Medical Device Recall · October 6, 2025
Liberta RC DBS IPG (Implantable Pulse Generator), Model Number 62400There is a potential issue affecting Eterna Spinal Cord Stimulation (SCS) Implantable Pulse Generators (IPGs), Model 32400 and Liberta RC Deep Brain Stimulation (DBS) Implantable Pulse Generators (IPGs), Model 62400 . These devicess may experience a loss of communication with the Clinician Programmer (CP) and/or the Patient Controller (PC).
- Class II
Drug Recall · October 6, 2025
Desipramine Hydrochloride Tablets, USP, 150 mg, 50 count bottle (NDC 23155-583-25), Rx only, Manufactured by: USV Private Limited, Daman, India, Manufactured for: Avet Pharmaceuticals Inc., East BrunsCGMP Deviations: N-Nitroso Desipramine impurity exceeding the permissible acceptable daily intake level.
- Class II
Food Recall · October 6, 2025
RICED CAULIFLOWER IQF NET WEIGHT: 30lbs (13.60 kg) PACK DATE: 08/04/2025 BEST BY: 08/04/2026 INGREDIENTS: CAULIFLOWER PERISHABLE KEEP FROZENPotential contamination with Listeria monocytogenes.
- Unclassified
Vehicle Recall · October 4, 2025
Volkswagen Group of America, Inc.
2025 VOLKSWAGEN ID. BUZZAn incorrectly displayed warning light can fail to alert the driver to critical safety information, increasing the risk of a crash.
- Class II
Food Recall · October 4, 2025
Jumbo Meat Ball Sub; Net Weight: 8.9oz; Product Code: Fresh Thru 10-15-25, 10/16/2025, 10/20/2025 In clear plastic packaging with white sticker labelMozzarella Cheese ingredient potential to be contaminated with metal shavings.
- Class II
Food Recall · October 3, 2025
Pizza style shredded cheese blend (containing low-moisture part-skim mozzarella and mild cheddar cheeses), individually packaged in a plastic bag as: 1) Econo Pizza - Shredded, 8 oz., UPC 893800297,Potential metal fragments from supplier raw material (downstream recall)
- Class I
Food Recall · October 3, 2025
Twin Marquis brand THICK SHANGHAI STYLE PLAIN NOODLE; NET WT 16 OZ; Ingredients: Bleached Wheat Flour, Water, Corn Starch, Salt, Sodium Benzoate (For Freshness); Contains: Wheat.; Produced on machinerProduct contains undeclared egg, FD&C Yellow 5, and FD&C Yellow 6.
- Class II
Food Recall · October 3, 2025
Happy Farms by Aldi Italian Style shredded cheese blend (containing low-moisture part-skim mozzarella, not-smoked provolone, romano, asiago & parmesan finely shredded cheeses), 12 oz., individually paPotential metal fragments from supplier raw material (downstream recall)
- Class II
Food Recall · October 3, 2025
Food Club Finely Shredded Pizza Style Four Cheese Blend (containing low-moisture part-skim mozzarella, not-smoked provolone, parmesan & romano cheeses), 8 oz., packaged individually in a plastic bag,Potential metal fragments from supplier raw material (downstream recall)
- Unclassified
Vehicle Recall · October 3, 2025
2024 HOLIDAY RAMBLER INVICTA, 2026 HOLIDAY RAMBLER INVICTAA propane gas leak increases the risk of a fire.
- Class II
Food Recall · October 3, 2025
COCACOLA SOUTHWEST BEVERAGES LLC
Coca-Cola Zero Sugar 12oz Can -12 pack 49000042559 / FEB0226MAA Coca-Cola Zero Sugar 12oz Can -35 pack 49000058499 / FEB0226MAAPotential presence of foreign material (metal) in the product
- Class I
Food Recall · October 3, 2025
Frozen Crab Paste; 3.5 OZ (100g); Imported by Mutual Tading Co. Inc. UPC# 72546723040 "Not for retail Sale" Frozen Crab Paste IM-2 in w/Tray; 500g; Imported by Mutual Trading Co. Inc. UPC# 7254660785Undeclared allergen ingredients (fish, soy, and wheat)