Hazard Type

Other Recalls

21,986 product recalls involving other. Search official CPSC, FDA, and USDA datasets for every recall issued due to this hazard.

21,986Total Recalls
1,733Critical
7708.6MUnits Affected
All Recalls

Every Other Recall

Sorted by most recent. Click any recall for full details and safety information.

21,986 recalls
High RiskFDA
Philips Medical Systems Nederlands
Mutlidiagnost-Eleva with Flat Detector Eleva with Flat Detector 708037 As a multifunctional universal imaging application system, Gen...
Diagnostic Devices·199 affected·Mar 26, 2018
High RiskFDA
Philips Medical Systems Nederlands
708033 URODiagnost As a multifunctional universal imaging application system, General RJF, Fluoroscopy, Radiography and Angiography ca...
Diagnostic Devices·20 affected·Mar 26, 2018
High RiskFDA
Ethicon Endo-surgery Inc
5mm Endopath Xcel with Optiview Technology, Universal Trocar with Stability Sleeve, 5mm, 75mm shaft length, 2CB5ST
Medical Devices·11,074 affected·Mar 26, 2018
High RiskFDA
Philips Medical Systems Nederlands
MultiDiagnost Eleva 708036 As a multifunctional universal imaging application system, General RJF, Fluoroscopy, Radiography and Angiog...
Diagnostic Devices·37 affected·Mar 26, 2018
High RiskFDA
Philips Medical Systems Nederlands
MultiDiagnostic-Eleva with Flat Detector 708035 As a multifunctional universal imaging application system, General RJF, Fluoroscopy, R...
Diagnostic Devices·1 affected·Mar 26, 2018
High RiskFDA
Ethicon Endo-surgery Inc
5mm Endopath Xcel with Optiview Technology, Universal Trocar with Stability Sleeve, 5mm, 100mm shaft length, 2CB5LT
Medical Devices·95,233 affected·Mar 26, 2018
High RiskFDA
Straumann Manufacturing, Inc.
Straumann¿ Emdogain 015, USA. Enamel Matrix Derivative. Article Number 075.099
Medical Devices·3,046 affected·Mar 23, 2018
High RiskFDA
Biomerieux Sa
The VITEK¿ 2 Anaerobic and Corynebacteria identification card (ANC) is intended for use with the VITEK¿ 2 Systems for the automated ident...
Diagnostic Devices·135 affected·Mar 23, 2018
High RiskFDA
Straumann Manufacturing, Inc.
Straumann¿ Emdogain 0.7 ml Multipack. Enamel Matrix Derivative. Article Number 075.116W
Medical Devices·1,084 affected·Mar 23, 2018
High RiskFDA
Straumann Manufacturing, Inc.
Straumann¿ Emdogain 0.3 ml Multipack USA. Enamel Matrix Derivative. Article Number 075.113
Medical Devices·2,816 affected·Mar 23, 2018
High RiskFDA
Biomerieux Sa
The VITEK 2 Gram-Positive identification card (GP) is intended for use with the VITEK 2 Systems for the automated identification of most ...
Diagnostic Devices·15 affected·Mar 23, 2018
High RiskFDA
Straumann Manufacturing, Inc.
Straumann¿ Emdogain 0.3 ml Multipack. Enamel Matrix Derivative. Article Number 075.114W
Medical Devices·2,915 affected·Mar 23, 2018
High RiskFDA
Volcano Corporation
Philips Volcano CORE M2 Vascular System, Part # 400-0100.17, Rx Only. Used for the qualitative and quantitative evaluation of vascular...
Medical Devices·8 affected·Mar 22, 2018
RecallFDA
Pepsi Beverage Co
diet Pepsi, 12 FL OZ, in aluminum cans packaged in 12 pk paper cartons
Food·1,972 affected·Mar 21, 2018
High RiskFDA
Bard Medical Division
Bard Midstream Urine Collector with Rigid Funnel and Iodophor Prep Pads. Product Packaging: Three (3) PVP-I prep pads are packed into ea...
Medical Devices·131,950 affected·Mar 21, 2018
High RiskFDA
Siemens Healthcare Diagnostics, Inc.
Dimension Vista¿ MULTI 2 SDIL, KD694, SMN# 10483586
Medical Devices·1,195 affected·Mar 21, 2018
High RiskFDA
Siemens Healthcare Diagnostics, Inc.
Dimension Vista¿ MULTI 1 SDIL, KD693, SMN# 10469971
Medical Devices·197 affected·Mar 21, 2018
RecallUSDA
California Jerky Factory, Inc.
California Jerky Factory, Inc. Recalls Beef Jerky Products Due to Possible Processing Deviation
Beef·0 affected·Mar 21, 2018
RecallUSDA
California Jerky Factory, Inc.
California Jerky Factory, Inc. Retira Productos De Carne Seca Debido A Una Posible Desviacin Durante El Procesamiento
Beef·0 affected·Mar 21, 2018
RecallFDA
Pepsi Cola Bottling Company
Diet Pepsi; NOW ASPARTAME FREE; 6 PACK; 16 OZ BOTTLES; 6-16 FLOZ BOTTLES (96 FL OZ)
Food·167 affected·Mar 20, 2018
High RiskFDA
Epic Extremity, Llc
Epic Extremity Plate System,10x10 Plate Caddy, Part 2111-1010 with 2.7 and 3.5mm Non-Locking Screw (2001-27XX-N & 2001-35XX-N)
Medical Devices·9 affected·Mar 20, 2018
High RiskFDA
Epic Extremity, Llc
Epic Extremity Plate System, Midfoot/Flatfoot Insert, Part 2111-0005 with Extended Butterfly Plate (2000-5002)
Medical Devices·6 affected·Mar 20, 2018
RecallUSDA
Mickey Brown, Inc.
Mickey Brown, Inc Recalls Beef Burrito Products Produced Without Benefit of Inspection
Beef·0 affected·Mar 20, 2018
RecallUSDA
Mickey Brown, Inc.
Mickey Brown, Inc Retira Productos De Burrito De Carne De Res Producidos Sin El Beneficio De La Inspeccin
Beef·0 affected·Mar 20, 2018
High RiskFDA
Teva Pharmaceuticals Usa
Estradiol Vaginal Inserts, USP 10 mcg, packaged in a) 8 inserts/carton (NDC 0093-3223-08) and b) 18 inserts/carton (NDC 0093-3223-97), Rx...
Drugs·640,486 affected·Mar 19, 2018
Medium RiskFDA
Glenmark Pharmaceuticals Inc., Usa
Indomethacin Capsules USP, 50 mg, 100-count bottle, Rx Only, Manufactured by: Glenmark Pharmaceuticals Ltd., Colvale-Bardez, Goa 403513, ...
Oral Drugs·109,080 affected·Mar 19, 2018
RecallFDA
Lake Erie Medical & Surgical Supply Inc
Tramadol Hydrochloride 50 mg tablets, 120-count, Rx Only; Distributed by Quality Care Products, Temperance, MI 48182 Mfr. CSPC Ouyl Pharm...
Oral Drugs·16 affected·Mar 19, 2018
High RiskFDA
Teleflex Medical Europe Ltd
Teleflex MEDICAL LMA(TM) MADgic(TM) LARYNGO-TRACHEAL MUCOSAL ATOMIZATION DEVICE, MAD700, QTY: 1 Intended for the application of topical a...
Medical Devices·25 affected·Mar 19, 2018
High RiskFDA
Hycor Biomedical Inc
HYTEC 288 System, Model 74007P, automated immunoanalyzer (EIA) instrument. For in vitro diagnostic use only. HYTEC AUTOSTAT II RF as...
Diagnostic Devices·288 affected·Mar 19, 2018
RecallFDA
Smucker Natural Foods, Inc.
SANTA CRUZ organic BLACKBERRY POMEGRANATE fruit spread NET WT 9.5 OZ (270 g) UPC 0 36192 10510 0
Produce·3,753 affected·Mar 16, 2018
RecallFDA
Smucker Natural Foods, Inc.
SANTA CRUZ organic APRICOT fruit spread NET WT 9.5 OZ (270 g) UPC 0 36192 10514 8
Produce·966 affected·Mar 16, 2018
RecallFDA
Smucker Natural Foods, Inc.
SANTA CRUZ organic MANGO fruit spread NET WT 9.5 OZ (270 g) UPC 0 36192 10516 2
Produce·2,537 affected·Mar 16, 2018
RecallFDA
Smucker Natural Foods, Inc.
SANTA CRUZ organic SEEDLESS RED RASPBERRY fruit spread NET WT 9.5 OZ (270 g) UPC 0 36192 10513 1
Produce·5,589 affected·Mar 16, 2018
RecallFDA
Smucker Natural Foods, Inc.
SANTA CRUZ organic STRAWBERRY fruit spread NET WT 9.5 OZ (270 g) UPC 0 36192 10515 5
Produce·11,369 affected·Mar 16, 2018
RecallFDA
Smucker Natural Foods, Inc.
SANTA CRUZ organic CONCORD GRAPE fruit spread NET WT 9.5 OZ (270 g) UPC 0 36192 10517 9
Produce·1,974 affected·Mar 16, 2018
High RiskFDA
Nobel Biocare Usa Llc
Nobel Biocare 17¿ Multi-Unit Abutment, Conical Connection NP, 2.5mm, REF 36614. Product Usage: Intended to be used in the upper and low...
Medical Implants·74 affected·Mar 16, 2018
High RiskFDA
Terumo Cardiovascular Systems Corporation
Sarns TCM II, Catalog Numbers: 4415; 4416;164925; 164930;164935;164940 UDI 00886799000014 The Sarns TCM is indicated for controlling a...
Medical Devices·2,393 affected·Mar 16, 2018
High RiskFDA
Ge Medical Systems Ultrasound & Primary Care Diagnostics, Ll
GE Healthcare Lunar: a) DPX NT, Model Numbers: LU8230, LU40338, LU42357, LU42369 b) DPX MD+, Model Numbers: LU8230, LU40338, LU40352 ...
Medical Devices·43 affected·Mar 16, 2018
CriticalFDA
Bayer Healthcare Pharmaceuticals, Inc.
All Alka-Seltzer Plus¿ packages with a full front panel instant Redeemable Coupon (IRC) affixed to the individual carton. The recalled pr...
Drugs·188,631 affected·Mar 15, 2018
RecallFDA
Invagen Pharmaceuticals, Inc.
buPROPion HCl Extended-Release Tablets, USP (SR), 150 mg ,a) 60 count (NDC 69097-878-03) and b) 100 count (NDC 69097-878-07) bottles, ...
Oral Drugs·0 affected·Mar 15, 2018
RecallFDA
Invagen Pharmaceuticals, Inc.
buPROPion HCl Extended-Release Tablets, USP (SR), 100 mg, 60 count bottles, Rx Only, Manufactured for: Cipla USA Inc. 1560 Sawgrass Cor...
Oral Drugs·0 affected·Mar 15, 2018
High RiskFDA
Teleflex Medical Europe Ltd
Simplastic Suprapubic Puncture Instruments: Product Code Equivalent Code (a) 650704100 551310 (b) 650704120 551312 ...
Medical Devices·4,220 affected·Mar 15, 2018
High RiskFDA
Teleflex Medical Europe Ltd
Rectal Catheters; Product Code Equivalent Code 580114 580114 Product Usage: Rectal Balloon Catheter is inserted into t...
Surgical Devices·6,340 affected·Mar 15, 2018
High RiskFDA
Teleflex Medical Europe Ltd
Latex Rebreathing Bags: Product Code Equivalent Code (a) 151174050 151174 (b) 153000005 153000005 (c) 153000010 153000010 (d) 153000...
Respiratory Devices·107,962 affected·Mar 15, 2018
High RiskFDA
Teleflex Medical Europe Ltd
Baker Jejunostomy Tubes: Product Code Equivalent Code (a) 655300160 655316 (b) 655500200 655520
Medical Devices·200 affected·Mar 15, 2018
RecallFDA
Pepsico Inc
diet pepsi caffeine free Classic Diet Pepsi Taste, 12 FL OZ (355 mL), UPC: 0 12000 17230 4
Food·194 affected·Mar 14, 2018
High RiskFDA
Philips Electronics North America Corporation
Allura Xper R8.x.25.5 and UNIZ systems (only with a FlexVision large screen monitor), Interventional fluoroscopic x-ray system Product...
Medical Implants·682 affected·Mar 14, 2018
High RiskFDA
Accelerate Diagnostics Inc
Accelerate PhenoTest BC kit, Ref #10101018. The firm name on the label is Accelerate Diagnostics, Tucson, AZ. A multiplexed in-vitro ...
Diagnostic Devices·95 affected·Mar 14, 2018